Company Name	Product Name	Main Body Diameter (mm)	Main Body Length (cm)	Main Body Delivery System Profile: Device OD (F)	Sheath Required for Delivery	Delivery Sheath OD (F)	Fixation Location	Stent Expansion	Stent Material	Graft Material	Comments
Medtronic	Endurant II AAA Stent Graft System	23, 25, 28, 32, 36	12.4, 14.5, 16.6	18, 20	No	–	Suprarenal	Self expanding	Nitinol	Woven polyester	Baseline configuration requires contralateral limb only; may be used in conjunction with the Heli-FX EndoAnchor System with short (≥ 4 mm and < 10 mm) infrarenal necks
Medtronic	Endurant II AUI Stent Graft System	23, 25, 28, 32, 36	10.2	18, 20	No	–	Suprarenal	Self expanding	Nitinol	Woven polyester	Includes all limbs
Medtronic	Endurant IIs AAA Stent Graft System	23, 25, 28, 32, 36	10.3	18, 20	No	–	Suprarenal	Self expanding	Nitinol	Woven polyester	Baseline configuration requires ipsilateral and contralateral limbs; may be used in conjunction with the Heli-FX EndoAnchor System with short (≥ 4 mm and < 10 mm) infrarenal necks

Company Name	Product Name	Iliac Limb Diameter (mm)	Iliac Limb Length (cm)	Comments
Medtronic	Endurant II AAA Stent Graft System	10, 13, 16, 20, 24, 28	8.2, 9.3, 12.4, 14.6, 15.6, 19.9*	*Inclusive of both ipsilateral and contralateral limbs
Medtronic	Endurant II AUI Stent Graft System	10, 13, 16, 20, 24, 28	8.2, 9.3, 12.4, 14.6, 15.6, 19.9*	*Includes all limbs
Medtronic	Endurant IIs AAA Stent Graft System	10, 13, 16, 20, 24, 28	8.2, 9.3, 12.4, 14.6, 15.6, 19.9*	*Reflects total limb length

Company Name	Product Name	Main Body Extensions Diameter (mm)	Main Body Extensions Length (cm)	Iliac Leg Extensions Diameter (mm)	Iliac Leg Extensions Length (cm)	Aorto-Uni-Iliac/Converter Proximal Diameter (mm)	Aorto-Uni-Iliac/Converter Length (cm)	Occluders Diameter (mm)	Comments
Medtronic	Endurant II AAA Stent Graft System	23, 25, 28, 32, 36	4.9, 7	10, 13, 20, 24, 28	8.2	23, 25, 28, 32, 36	10.2	–	–

Company Name	Product Name	Components	Sizes	Description	US FDA Indicated Use
Medtronic	Heli-FX EndoAnchor System	Heli-FX Guide	Deflecting tip lengths: 22, 28 mm; 16-F OD; 62-cm working length; 0.035-inch wire compatible	Deflecting guide catheter used to position Heli-FX Applier to implant EndoAnchors	Indicated for use in patients whose endografts have exhibited migration or endoleak, or are at risk of such complications, in whom augmented fixation and/or sealing is required to regain or maintain adequate aneurysm exclusion; evaluated via in vitro testing and determined to be compatible with the Cook Zenith, Cook Zenith TX2, Gore Excluder, Gore TAG, Medtronic AneuRx, Medtronic Endurant, Medtronic Talent AAA, Medtronic Talent TAA, Medtronic Valiant Xcelerant, Medtronic Valiant Captivia, and Medtronic Valiant Navion endografts; use with other endografts has not been evaluated
Medtronic	Heli-FX EndoAnchor System	Heli-FX Applier with EndoAnchor cassette (contains 10 EndoAnchors)	12-F OD; 86-cm working length	Battery-operated delivery system with two-stage EndoAnchor deployment with repositioning capability	Indicated for use in patients whose endografts have exhibited migration or endoleak, or are at risk of such complications, in whom augmented fixation and/or sealing is required to regain or maintain adequate aneurysm exclusion; evaluated via in vitro testing and determined to be compatible with the Cook Zenith, Cook Zenith TX2, Gore Excluder, Gore TAG, Medtronic AneuRx, Medtronic Endurant, Medtronic Talent AAA, Medtronic Talent TAA, Medtronic Valiant Xcelerant, Medtronic Valiant Captivia, and Medtronic Valiant Navion endografts; use with other endografts has not been evaluated
Medtronic	Heli-FX EndoAnchor System	Ancillary EndoAnchor Cassette (contains five EndoAnchors)	0.5-mm round wire; 3-mm diameter X 4.5-mm length helix	Implants are designed to provide independent transmural sealing and fixation of an endograft to the aortic wall	Indicated for use in patients whose endografts have exhibited migration or endoleak, or are at risk of such complications, in whom augmented fixation and/or sealing is required to regain or maintain adequate aneurysm exclusion; evaluated via in vitro testing and determined to be compatible with the Cook Zenith, Cook Zenith TX2, Gore Excluder, Gore TAG, Medtronic AneuRx, Medtronic Endurant, Medtronic Talent AAA, Medtronic Talent TAA, Medtronic Valiant Xcelerant, Medtronic Valiant Captivia, and Medtronic Valiant Navion endografts; use with other endografts has not been evaluated

Company Name	Product Name	Diameter (inch)	Length (cm)	Flexible Tip Length (cm)
Medtronic	Steerant Super Stiff Guidewire	0.035	200, 260	15

Company Name	Product Name	Components	Sizes	Description	US FDA Indicated Use
Medtronic	Heli-FX Thoracic EndoAnchor System	Heli-FX Guide	Deflecting tip lengths: 22, 32, 42 mm; 18-F OD; 90-cm working length; 0.035-inch wire compatible	Deflecting guide catheter used to position Heli-FX Applier to implant EndoAnchors	Indicated for use in patients whose endografts have exhibited migration or endoleak, or are at risk of such complications, in whom augmented fixation and/or sealing is required to regain or maintain adequate aneurysm exclusion; evaluated via in vitro testing and determined to be compatible with the Cook Zenith, Cook Zenith TX2, Gore Excluder, Gore TAG, Medtronic AneuRx, Medtronic Endurant, Medtronic Talent AAA, Medtronic Talent TAA, Medtronic Valiant Xcelerant, Medtronic Valiant Captivia, and Medtronic Valiant Navion endografts; use with endografts other than those listed above has not been evaluated
Medtronic	Heli-FX Thoracic EndoAnchor System	Ancillary EndoAnchor Cassette (contains five EndoAnchors)	0.5-mm round wire; 3-mm diameter X 4.5-mm length helix	Helical EndoAnchor implants designed to provide independent transmural sealing and fixation of an endograft to the aortic wall	Indicated for use in patients whose endografts have exhibited migration or endoleak, or are at risk of such complications, in whom augmented fixation and/or sealing is required to regain or maintain adequate aneurysm exclusion; evaluated via in vitro testing and determined to be compatible with the Cook Zenith, Cook Zenith TX2, Gore Excluder, Gore TAG, Medtronic AneuRx, Medtronic Endurant, Medtronic Talent AAA, Medtronic Talent TAA, Medtronic Valiant Xcelerant, Medtronic Valiant Captivia, and Medtronic Valiant Navion endografts; use with endografts other than those listed above has not been evaluated
Medtronic	Heli-FX Thoracic EndoAnchor System	Heli-FX Applier with EndoAnchor cassette (contains 10 EndoAnchors)	12-F OD; 114-cm working length	Battery-operated delivery system with two-stage EndoAnchor deployment with repositioning capability	Indicated for use in patients whose endografts have exhibited migration or endoleak, or are at risk of such complications, in whom augmented fixation and/or sealing is required to regain or maintain adequate aneurysm exclusion; evaluated via in vitro testing and determined to be compatible with the Cook Zenith, Cook Zenith TX2, Gore Excluder, Gore TAG, Medtronic AneuRx, Medtronic Endurant, Medtronic Talent AAA, Medtronic Talent TAA, Medtronic Valiant Xcelerant, Medtronic Valiant Captivia, and Medtronic Valiant Navion endografts; use with endografts other than those listed above has not been evaluated

Company Name	Product Name	Drug Type	Drug Concentration (µg/mm2)	Excipient Type	Guidewire Compatibility (inch)	Shaft Length (cm)	Sheath Compatibility (F)	Balloon Diameters (mm)	Balloon Lengths (mm)	US FDA Indicated Use
Medtronic	In.Pact 018	Paclitaxel	3.5	Urea	0.018	130, 200	5 (4–6 mm), 6 (7 mm)	4, 5, 6, 7	40, 60, 80, 100, 120, 150	Indicated for percutaneous transluminal angioplasty, after appropriate vessel preparation, of de novo, restenotic, or in-stent restenotic lesions with lengths up to 360 mm in superficial femoral or popliteal arteries with reference vessel diameters of 4 to 7 mm
Medtronic	In.Pact Admiral	Paclitaxel	3.5	Urea	0.035	80, 130	5 (4 mm), 6 (5, 6 mm), 7 (7 mm)	4, 5, 6, 7	40, 60, 80, 120, 150, 200, 250	Indicated for PTA, after appropriate vessel preparation, of de novo, restenotic, or in-stent restenotic lesions with lengths up to 360 mm in superficial femoral or popliteal arteries with reference vessel diameters of 4 to 7 mm

Company Name	Product Name	Nominal Pressure (atm)	Rated Burst Pressure (atm)	Guidewire Compatibility (inch)	Shaft Length (cm)	Sheath Compatibility (F)	Balloon Diameters (mm)	Balloon Lengths (cm)
Medtronic	Admiral Xtreme OTW PTA Balloon Catheter	6, 8	Up to 14	0.035	80, 130	5–7	4, 5, 6, 7	20, 25, 30
Medtronic	Chameleon High-Pressure PTA Balloon	12, 14	14, 18, 22, 25	0.035	75	6, 7, 8	5, 6, 7, 8, 9, 10, 12	4
Medtronic	Chocolate PTA Dilatation Catheter	6 (5–6 mm), 9 (2.5–4 mm)	12 (5–6 mm), 14 (2.5–4 mm)	0.014 (2.5–4 mm), 0.018 (5–6 mm)	120 (5–6 mm), 135 (3.5–4 mm), 150 (2.5, 3 mm)	5 (2.5–4 mm), 6 (5–6 mm)	2.5, 3, 3.5, 4, 5, 6	4, 8, 12
Medtronic	EverCross 0.035 PTA Balloon	7, 8, 10	Up to 20	0.035	40, 80, 135	5, 6, 7	3, 4, 5, 6, 7, 8, 9, 10, 12	2, 3, 4, 6, 8, 10, 12, 15, 20
Medtronic	Fortrex 0.035 OTW PTA Balloon Catheter	7, 8, 9, 12	Up to 24	0.035	40, 80, 135	6, 7	4, 5, 6, 7, 8, 9, 10, 12	2, 4, 8, 10
Medtronic	NanoCross Elite 0.014 PTA Balloon	7, 8, 10	14	0.014	90, 150	4	1.5, 2, 2.5, 3, 3.5, 4, 5, 6	2, 4, 8, 12, 15, 21
Medtronic	Pacific Plus	8	Up to 22	0.018	90, 150, 200	4, 5	2, 2.5, 3, 3.5, 4, 5, 6, 7	2, 4, 6, 8, 10, 12, 15, 20, 25, 30
Medtronic	RapidCross 0.014 RX PTA Balloon	8	14	0.014	90, 170	4	1.5, 2, 2.5, 3, 3.5, 4	2, 4, 6, 8, 10, 12, 15, 21

Company Name	Product Name	Nominal Pressure (atm)	Rated Burst Pressure (atm)	Guidewire Compatibility (inch)	Size (F)	Sheath Compatibility (F)	Shaft Length (cm)	Balloon Diameters (mm)	Balloon Lengths (cm)
Medtronic	Chocolate PTA Dilatation Catheter	6 (5–6 mm), 9 (2.5–4 mm)	10 (5–6 mm), 14 (2.5–4 mm)	0.014 (2.5–4 mm), 0.018 (5–6 mm)	–	5 (2.5–4 mm), 6 (4.5–6 mm)	120 (5–6 mm), 135 (3.5–4 mm), 150 (2.5, 3 mm)	2.5, 3, 3.5, 4, 5, 6	4, 8, 12

Company Name	Product Name	Proximal OD (F)	Distal OD (F)	Tip Length (mm)	Balloon Diameters (mm)	Balloon Lengths (mm)
Medtronic	HyperForm Occlusion Balloon System	2.8	2.2	2	3, 4	7, 15
Medtronic	HyperForm Occlusion Balloon System	2.8	2.5	2	4	15, 20
Medtronic	HyperForm Occlusion Balloon System	2.8	3	2	7	7, 15
Medtronic	HyperGlide Occlusion Balloon System	2.8	2.2	4	3	10, 15
Medtronic	HyperGlide Occlusion Balloon System	2.8	2.2	4	4	10, 15, 20, 30
Medtronic	HyperGlide Occlusion Balloon System	2.8	2.2	4	5	15, 20, 30

Company Name	Product Name	Type	Size (F)	Length (cm)	Internal Diameter (inch)	Radiopaque Tip (Yes/No)	Hydrophilic Coated
Medtronic	Launcher	Braided	6	47, 55, 100	0.071	No (radiopaque markerband 3 mm from the tip)	Yes
Medtronic	Launcher	Braided	7	47, 55, 100	0.081	No (radiopaque markerband 3 mm from the tip)	Yes
Medtronic	Launcher	Braided	8	47, 55, 100	0.090	No (radiopaque markerband 3 mm from the tip)	Yes
Medtronic	Navien Intracranial Support Catheter	–	5	105, 115, 125, 130	0.058	Yes	Yes
Medtronic	Navien Intracranial Support Catheter	–	6	95, 105, 115, 125, 130	0.072	Yes	Yes
Medtronic	Sherpa NX Balanced	Braided	6	47, 55, 100	0.070	No (radiopaque markerband 3 mm from the tip)	Yes
Medtronic	Sherpa NX Balanced	Braided	7	47, 55, 100	0.080	No (radiopaque markerband 3 mm from the tip)	Yes
Medtronic	Launcher	Braided	5	47, 55, 100	0.058	Yes	No

Company Name	Product Name	Catheter Size (F)	Working Length (cm)	Minimum Guiding Catheter ID (inch)	Comments
Medtronic	TrailBlazer Angled Support Catheter	4 (0.035-inch wire)	65, 90, 135, 150	0.055	A braided, low-profile hydrophilic catheter that provides optimized support for increased pushability in difficult-to-access and -cross lesions
Medtronic	TrailBlazer Angled Support Catheter	2.6 (0.018-inch wire)	90, 135, 150	0.055	A braided, low-profile hydrophilic catheter that provides optimized support for increased pushability in difficult-to-access and -cross lesions
Medtronic	TrailBlazer Angled Support Catheter	2.3 (0.014-inch wire)	90, 135, 150	0.055	A braided, low-profile hydrophilic catheter that provides optimized support for increased pushability in difficult-to-access and -cross lesions
Medtronic	TrailBlazer Support Catheter	4 (0.018-inch wire)	90, 135, 150	0.045	A seamless, low-profile hydrophilic catheter that provides optimized support for increased pushability in difficult-to-cross lesions
Medtronic	TrailBlazer Support Catheter	4 (0.014-inch wire)	135, 150	0.045	A seamless, low-profile hydrophilic catheter that provides optimized support for increased pushability in difficult-to-cross lesions
Medtronic	TrailBlazer Support Catheter	5 (0.035-inch wire)	65, 90, 135, 150	0.066	A seamless, low-profile hydrophilic catheter that provides optimized support for increased pushability in difficult-to-cross lesions

Company Name	Product Name	Materials Used	Coil Type	Method of Detachment	US FDA Indicated Use	Comments
Medtronic	Axium Detachable Coils	Implant material: platinum detachable coils	Framing, filling, finishing	Instant detachment (mechanical)	Intended for the endovascular embolization of intracranial aneurysms; also intended for the embolization of other neurovascular abnormalities such as AVMs and AVFs	–
Medtronic	Axium MicroFX Detachable Coils	Implant material: platinum detachable coils with PGLA or nylon filaments	Framing, filling, finishing	Instant detachment (mechanical)	Intended for the endovascular embolization of intracranial aneurysms; also intended for the embolization of other neurovascular abnormalities such as AVMs and AVFs	–
Medtronic	Axium Prime Detachable Coils	Implant material: platinum detachable coils	Framing, filling, finishing	Instant detachment (mechanical)	Intended for the endovascular embolization of intracranial aneurysms; also intended for the embolization of other neurovascular abnormalities such as AVMs and AVFs	–
Medtronic	Axium Prime Detachable Coils (Extra Soft)	Implant material: platinum detachable coils	Framing, filling, finishing	Instant detachment (mechanical)	Intended for the endovascular embolization of intracranial aneurysms; also intended for the embolization of other neurovascular abnormalities such as AVMs and AVFs	–

Company Name	Product Name	Type (Detachable, Pushable)	Material	Coil Diameter (mm)	Coil Length (cm)	Recommended Delivery Catheter Sizes (ID) (inch)	US FDA Indicated Use
Medtronic	Concerto Nylon Fibered Helical Coils	Detachable	–	5	15, 20	0.021	Indicated for arterial and venous embolizations in the peripheral vasculature
Medtronic	Concerto Nylon Fibered Helical Coils	Detachable	–	2	4, 6, 8	0.017	Indicated for arterial and venous embolizations in the peripheral vasculature
Medtronic	Concerto Nylon Fibered Helical Coils	Detachable	–	3	4, 8	0.017	Indicated for arterial and venous embolizations in the peripheral vasculature
Medtronic	Concerto Nylon Fibered Helical Coils	Detachable	–	4	8, 10	0.017	Indicated for arterial and venous embolizations in the peripheral vasculature
Medtronic	Concerto Nylon Fibered Helical Coils	Detachable	–	6	20	0.021	Indicated for arterial and venous embolizations in the peripheral vasculature
Medtronic	Concerto Nylon Fibered Helical Coils	Detachable	–	7, 8, 9, 10	30	0.021	Indicated for arterial and venous embolizations in the peripheral vasculature
Medtronic	Concerto PGLA Fibered 3D Coils	Detachable	–	6	20	0.017	Indicated for arterial and venous embolizations in the peripheral vasculature
Medtronic	Concerto PGLA Fibered 3D Coils	Detachable	–	12, 14, 16, 18	40	0.021	Indicated for arterial and venous embolizations in the peripheral vasculature
Medtronic	Concerto PGLA Fibered 3D Coils	Detachable	–	2	2, 4, 6	0.017	Indicated for arterial and venous embolizations in the peripheral vasculature
Medtronic	Concerto PGLA Fibered 3D Coils	Detachable	–	3	4, 6, 8	0.017	Indicated for arterial and venous embolizations in the peripheral vasculature
Medtronic	Concerto PGLA Fibered 3D Coils	Detachable	–	4	8, 10, 12	0.017	Indicated for arterial and venous embolizations in the peripheral vasculature
Medtronic	Concerto PGLA Fibered 3D Coils	Detachable	–	7, 8, 9, 10	30	0.017	Indicated for arterial and venous embolizations in the peripheral vasculature
Medtronic	Concerto PGLA Fibered 3D Coils	Detachable	–	5	15	0.017	Indicated for arterial and venous embolizations in the peripheral vasculature
Medtronic	Concerto PGLA Fibered Helical Coils	Detachable	–	12, 14	30	0.021	Indicated for arterial and venous embolizations in the peripheral vasculature
Medtronic	Concerto PGLA Fibered Helical Coils	Detachable	–	16, 18	40	0.021	Indicated for arterial and venous embolizations in the peripheral vasculature
Medtronic	Concerto PGLA Fibered Helical Coils	Detachable	–	20	50	0.021	Indicated for arterial and venous embolizations in the peripheral vasculature

Company Name	Product Name	Materials Used	US FDA Indicated Use	Comments
Medtronic	Onyx HD-500	EVOH, dimethyl sulfoxide, tantalum	Treating intracranial, saccular, sidewall aneurysms that present with a wide neck (≥ 4 mm) or with a dome-to-neck ratio < 2 mm that are not amenable to treatment with surgical clipping	High-viscosity formulation liquid embolic for the treatment of intracranial wide-necked aneurysms that are not amenable to treatment with surgical clipping
Medtronic	Onyx Liquid Embolic System: Onyx 18 and Onyx 34	EVOH, dimethyl sulfoxide, tantalum	Presurgical embolization of brain AVMs	An ethylene vinyl alcohol copolymer that provides controlled injection and reliability for presurgical embolization of brain AVMs

Company Name	Product Name	Material	Target Vessel Diameter (mm)	Delivery Wire Length (cm)	Recommended Catheter Sizes: ID (inch) or OD (F)	US FDA Indicated Use
Medtronic	MVP-3 Micro Vascular Plug System	Implant material: nitinol and PTFE	1.5–3	180	Microcatheter: 0.021	To obstruct or reduce the rate of blood flow in the peripheral vasculature
Medtronic	MVP-5 Micro Vascular Plug System	Implant material: nitinol and PTFE	3–5	180	Microcatheter: 0.027	To obstruct or reduce the rate of blood flow in the peripheral vasculature
Medtronic	MVP-7 Micro Vascular Plug System	Implant material: nitinol and PTFE	5–7	165	0.041 (4 F)	To obstruct or reduce the rate of blood flow in the peripheral vasculature
Medtronic	MVP-9 Micro Vascular Plug System	Implant material: nitinol and PTFE	7–9	165	Catheter: 0.043 (5 F)	To obstruct or reduce the rate of blood flow in the peripheral vasculature

Company Name	Product Name	Size (F)	Length (cm)	Guidewire Compatibility (inch)	Curved or Straight	Radiopaque Tip	Type of Special Access
Medtronic	TourGuide Steerable Sheath	6.5, 7, 8.5	Deflection lengths: 9, 17, 22 (mm); working lengths: 45, 55, 90	0.035, 0.038 (guidewire not included)	Deflectable to 180°	Yes	Steerable sheath that allows for quick access of challenging anatomy and delivery of peripheral vascular products

Company Name	Product Name	Size (F)	Length (cm)	Guidewire Compatibility (inch)	Curved or Straight	Radiopaque Tip
Medtronic	Fubuki Sheath	6, 7, 8	80, 90, 100, 110	–	Angled, straight	–
Medtronic	Sentrant Introducer Sheath With Hydrophilic Coating	12, 14, 16, 18, 20, 22, 24, 26	28, 64	0.035	Straight	Yes

Company Name	Product Name	Material Used	Maximum Guidewire Size (inch)	Introducer Size (F)	Stent Diameter (mm)	Stent Length (mm)	Delivery System Length (cm)	US FDA Indicated Use
Medtronic	IntraStent LD DoubleStrut (Unmounted) Stent System	316L stainless steel	–	8	9, 10, 11, 12	16, 26, 36, 56, 76	–	Biliary
Medtronic	IntraStent LD Max (Unmounted) Stent System	316L stainless steel	–	11	12	16, 26, 36	–	Biliary
Medtronic	IntraStent LD Mega (Unmounted) Stent System	316L stainless steel	–	9	9, 10, 11, 12	16, 26, 36	–	Biliary
Medtronic	ParaMount Mini GPS Stent System	316L stainless steel	0.014, 0.018	5 (5–6 mm), 6 (7 mm)	5, 6, 7	14, 18, 21	80	Biliary
Medtronic	Visi-Pro Stent System	316L stainless steel	0.035	6 (5–8 mm), 7 (9–10 mm)	5, 6, 7, 8, 9, 10	12 (5–7-mm diameters), 17, 27, 37, 57	80, 135	Biliary, iliac

Company Name	Product Name	Tapered Stent Diameters (Proximal/Distal) (mm)	Tapered Stent Lengths (mm)	Straight Stent Diameters (mm)	Straight Stent Lengths (mm)	Embolic Protection Device	Type	Position	US FDA Indicated Use
Medtronic	Protégé RX Carotid Stent System	8/6, 10/7	30, 40	6, 7, 8, 9, 10	20, 30, 40, 60	SpiderFX Embolic Protection Device	Filter: guidewire of choice	Distal	Used in conjunction with the SpiderFX embolic protection device, is indicated for the treatment of patients at high risk for adverse events from carotid endarterectomy who require percutaneous carotid revascularization and meet the following criteria: patients with carotid artery stenosis (≥ 50% for symptomatic patients by ultrasound or angiography or ≥ 80% for asymptomatic patients by ultrasound or angiography) of the common or internal carotid artery, and patients must have a reference vessel diameter within the range of 4.5–9.5 mm at the target lesion

Company Name	Product Name	Material Used	Introducer Size (F)	Guidewire Compatibility (inch)	Stent Diameter (mm)	Stent Length (mm)	Delivery System Length (cm)	US FDA Indicated Use
Medtronic	EverFlex Self-Expanding Peripheral Stent System	Nitinol	6	0.035	6, 7, 8	20, 30, 40, 60, 80, 100, 120	80, 120	Iliac
Medtronic	EverFlex Self-Expanding Peripheral Stent System	Nitinol	6	0.035	6, 7, 8	20, 30, 40, 60, 80, 100, 120, 150, 200	80, 120	SFA, PPA
Medtronic	EverFlex Self-Expanding Peripheral Stent With Entrust Delivery System	Nitinol	5	0.035	6, 7, 8	20, 40, 60, 80, 100, 120, 150	80, 120, 150	SFA/PPA
Medtronic	Protege EverFlex Self-Expanding Stent System	Nitinol	6	0.035	5	20, 30, 40, 60, 80, 100, 120	80, 120	Biliary
Medtronic	Protege GPS Self-Expanding Peripheral Stent System	Nitinol	6	0.035	9, 10, 12	20, 30, 40, 60, 80	80, 120	Iliac
Medtronic	Protege GPS Self-Expanding Stent System	Nitinol	6	0.035	9, 10, 12, 14	20, 30, 40, 60, 80	80, 120	Biliary

Company Name	Product Name	Stent Material	Cell Design	Introducer Size (F)	Guidewire Compatibility (inch)	Stent Diameter (mm)	Stent Length (mm)	Delivery System	Delivery System Length (cm)
Medtronic	Abre Venous Self-Expanding Stent System	Nickle-titanium alloy (nitinol)	Open-cell	9	0.035	10, 12, 14, 16, 18, 20	40, 60, 80, 100, 120, 150	Triaxial, thumbwheel	90

Company Name	Product Name	Type	Diameter (inch)	Length (cm)	Tip Type	Antithrombogenic	Comments
Medtronic	Wholey Guidewire System: Extension System	Fixed core	0.035	155	Straight/shapeable	PTFE coated	Supportive wire with soft, shapeable tip designed for atraumatic negotiation of the vasculature; core-to-tip design
Medtronic	Wholey Guidewire System: Floppy Tip, Exchange Length	Fixed core	0.035	260, 300	Straight/shapeable	PTFE coated	Supportive wire with soft, shapeable tip designed for atraumatic negotiation of the vasculature; core-to-tip design
Medtronic	Wholey Guidewire System: Floppy Tip, Extension Compatible	Fixed core	0.035	145, 175	Straight/shapeable	PTFE coated	Supportive wire with soft, shapeable tip designed for atraumatic negotiation of the vasculature; core-to-tip design
Medtronic	Wholey Guidewire System: Modified J Tip, Exchange Length	Fixed core	0.035	260, 300	Modified J/shapeable	PTFE coated	Supportive wire with soft, shapeable tip designed for atraumatic negotiation of the vasculature; core-to-tip design
Medtronic	Wholey Guidewire System: Modified J Tip, Extension Compatible	Fixed core	0.035	145, 175	Straight/shapeable, modified J/shapeable	PTFE coated	Supportive wire with soft, shapeable tip designed for atraumatic negotiation of the vasculature; core-to-tip design
Medtronic	Wholey Guidewire System: Standard Tip, Exchange Length	Fixed core	0.035	260, 300	Straight/shapeable	PTFE coated	Supportive wire with soft, shapeable tip designed for atraumatic negotiation of the vasculature; core-to-tip design
Medtronic	Wholey Guidewire System: Standard Tip, Extension Compatible	Fixed core	0.035	145, 175	Modified J/shapeable, straight/shapeable	PTFE coated	Supportive wire with soft, shapeable tip designed for atraumatic negotiation of the vasculature; core-to-tip design

Company Name	Product Name	Type	Diameter (inch)	Length (cm)	Tip Type	Comments
Medtronic	Avigo .014” Hydrophilic Guidewire	Stainless steel	0.014	205	Shapeable tip	–
Medtronic	Mirage .008” Hydrophilic Guidewire	Stainless steel	0.012 > 0.008	200	Shapeable tip	–
Medtronic	Silverspeed .010 Hydrophilic Guidewire	Stainless steel	0.010	200	Shapeable tip	–
Medtronic	Silverspeed .014 Hydrophilic Guidewire	Stainless steel	0.014	175, 200	Shapeable tip	–
Medtronic	X-Celerator Hydrophilic Exchange Guidewire	Stainless steel	0.010, 0.014	300, 350	Shapeable tip	–
Medtronic	X-Pedion .010 Hydrophilic Guidewires	Stainless steel	0.012 > 0.010	200	Shapeable tip	–
Medtronic	X-Pedion .014 Hydrophilic Guidewires	Stainless steel	0.014	200	Shapeable tip	–
Medtronic	F14 and F18 Peripheral Guidewires	Stainless steel	0.014, 0.018	300, 400	Straight and shapeable tip	10 specialty and workhorse wires; multiple tip loads and a mix of polymer jackets or coils

Company Name	Product Name	Type	Diameter (inch)	Length (cm)	Tip Type	Coating Type	Comments
Medtronic	Babywire Guidewire	Nitinol	0.012	18, 50	Straight	No	Assist in placement of IV catheters and exchange of small vessel arterial/venous lines
Medtronic	Nitrex Guidewire	Nitinol	0.014, 0.018, 0.025	60, 80, 180, 300 (0.018 inch); 80, 180, 300 (0.014 inch); 180, 260 (0.025 inch)	Angled: 0.014; straight, angled: 0.018, 0.025	Silicone	Solid nitinol core for 1:1 torque and kink resistance; silicone coating for lubricity and gold tungsten coils for enhanced visualization
Medtronic	Nitrex Guidewire With Flexible Shaft	Nitinol	0.035	145, 180, 260, 400	Straight, angled	Silicone	Solid nitinol core for 1:1 torque and kink resistance; silicone coating for lubricity and gold tungsten coils for enhanced visualization
Medtronic	Nitrex Guidewire With Stiff Shaft	Nitinol	0.035	80, 145, 180, 260, 300, 400	Straight, angled	Silicone	Solid nitinol core for 1:1 torque and kink resistance; silicone coating for lubricity and gold tungsten coils for enhanced visualization

Company Name	Product Name	Technology (RF, Microwave, Cryo, IRE)	Ex Vivo Ablation Zone	In Vivo Ablation Zone	Antenna/Electrode Length (cm)	Antenna Gauge	US FDA Indicated Use
Medtronic	Cool-tip	RF	20-mm active tip: up to 2.3 X 2.6 cm (one electrode); 25-mm active tip: up to 4.2 X 4.5 cm (three electrodes); 30-mm active tip: up to 3.1 X 3.7 cm (one electrode); 30-mm active tip: up to 5.5 X 5.2 cm (three electrodes); 40-mm active tip: up to 6.7 X 6.5 cm (three electrodes)	–	10, 15, 20, 25	17	Intended for use in percutaneous, laparoscopic, and intraoperative coagulation and ablation of tissue, such as partial or complete ablation of nonresectable liver tumors and osteoid osteoma tumors within bone
Medtronic	Emprint	Microwave	Up to 3.7 X 4.1 cm in lung (single antenna); up to 4.2 X 4.2 cm in liver (single antenna)	Up to 3.5 X 4 cm in liver (single antenna); up to 3.8 X 4.3 cm in lung (single antenna)	15, 20, 30	13	Intended for use in percutaneous, laparoscopic, and intraoperative coagulation (ablation) of soft tissue, including partial or complete ablation of nonresectable liver tumors; not intended for use in cardiac procedures
Medtronic	OsteoCool	RF	7-mm active tip: up to 1.1 X 1 cm (one electrode); 10-mm active tip: up to 1.7 X 1.3 cm (one electrode); 15-mm active tip: up to 2.3 X 1.8 cm (one electrode); 20-mm active tip: up to 2.9 X 2.1 cm (one electrode)	–	19	17	Intended for palliative treatment in spinal procedures by ablation of metastatic malignant lesions in a vertebral body; also intended for coagulation and ablation of tissue in bone during surgical procedures, including palliation of pain associated with metastatic lesions involving bone in patients who have failed or are not candidates for standard therapy

Company Name	Product Name	Minimum Vessel Diameter (mm)	Sheath Compatibility (F)	Crossing Profile (inch)	Working Length (cm)	Tip Length (cm)
Medtronic	HawkOne LS Directional Atherectomy System	3.5–7	7	0.104 (2.6 mm)	114	6.6
Medtronic	HawkOne LX Directional Atherectomy System	3.5–7	7	0.104 (2.6 mm)	114	9.6
Medtronic	HawkOne M Directional Atherectomy System	3–7	6	0.085 (2.2 mm)	135	5.9
Medtronic	HawkOne S Directional Atherectomy System	2–4	6	0.085 (2.2 mm)	151	5.9
Medtronic	SilverHawk DS Peripheral Plaque Excision System	1.5–2	6	0.073 (1.9 mm)	135	2.6
Medtronic	SilverHawk EXL Peripheral Plaque Excision System	2–3	6	0.080 (2 mm)	135	6

Company Name	Product Name	Catheter Size (F)	Wire Size (inch)	Working Length (cm)	Minimum Guiding Catheter ID (inch)	Comments
Medtronic	Enteer Re-entry System, Catheter	4.8	0.018	135, 150	0.066	Re-entry catheter designed with a unique flat balloon to self-orient in the subintimal space and easily target the true lumen using the Enteer Guidewire; catheter available in two sizes for above- and below-the-knee use
Medtronic	Enteer Re-entry System, Guidewire	–	0.014	300	–	Specialized guidewire designed to target Enteer catheter exit ports and engage and penetrate tissue for re-entry into the true lumen from a subintimal position; available in three levels of stiffness (flexible, standard, stiff) for use across a range of peripheral vessels
Medtronic	TrailBlazer Angled Support Catheter	2.6	0.018	90, 135, 150	0.055	A braided, low-profile hydrophilic catheter that provides optimized support for increased pushability in difficult to access and cross lesions
Medtronic	TrailBlazer Angled Support Catheter	4	0.035	65, 90, 135, 150	0.055	A braided, low-profile hydrophilic catheter that provides optimized support for increased pushability in difficult to access and cross lesions
Medtronic	TrailBlazer Angled Support Catheter	2.3	0.014	90, 135, 150	0.055	A braided, low-profile hydrophilic catheter that provides optimized support for increased pushability in difficult to access and cross lesions
Medtronic	TrailBlazer Support Catheter	5	0.035	65, 90, 135, 150	0.066	A seamless, low-profile catheter that provides optimized support for increased pushability in difficult to cross lesions
Medtronic	TrailBlazer Support Catheter	4	0.014	135, 150	0.045	A seamless, low-profile catheter that provides optimized support for increased pushability in difficult to cross lesions
Medtronic	TrailBlazer Support Catheter	4	0.018	90, 135, 150	0.045	A seamless, low-profile catheter that provides optimized support for increased pushability in difficult to cross lesions
Medtronic	Viance Crossing Catheter	2.9	0.014	150	0.066	Low-profile peripheral CTO crossing catheter with atraumatic distal tip; device operates via physician-controlled torque handle for fast manual spinning; the spinning motion created by the torque device allows the catheter tip to find its way through the lesion; available in flexible and standard stiffness

Company Name	Product Name	Size (F)	Tip-to-Cuff Insertion Length (cm)	Tip Type	Number of Lumens	Sideholes (Yes/No)	Coated (Yes/No)	Acute or Chronic
Medtronic	Argyle 8-F Single Lumen Catheter Straight Extension Catheter	8	15, 19.5	Tapered	Single	Yes	No	Acute
Medtronic	Argyle Peritoneal Dialysis Catheters	15	62.5, 112.3	PD	Single	Yes	No	PD
Medtronic	Mahurkar 12-F High Pressure Flow Pre-Curved Catheters	12	13, 16, 20, 24	Tapered	Triple	Yes	No	Acute
Medtronic	Mahurkar 13.5-F High Flow Catheters	13.5	13.5, 16, 19.5, 24	Tapered	Dual	Yes	No	Acute
Medtronic	Mahurkar 13.5-F High Flow Pre-Curved Catheters	13.5	13.5, 16, 19.5, 24	Tapered	Dual	Yes	No	Acute
Medtronic	Mahurkar Chronic Carbothane Dual Lumen Catheter	14.5	19, 23, 28, 33	Staggered	Dual	Yes	No	Chronic
Medtronic	Mahurkar Curved Extension Dual Lumen Catheter	11.5	13.5, 16, 19.5	Tapered	Dual	Yes	No	Acute
Medtronic	Mahurkar Curved Extension Dual Lumen Catheter IC Safety Trays	11.5	13.5, 16, 19.5, 24	Tapered	Dual	Yes	No	Acute
Medtronic	Mahurkar Curved Extension Dual Lumen Catheter Kits	8, 10, 11.5	12, 15, 19.5	Tapered	Dual	Yes	No	Acute
Medtronic	Mahurkar Elite Dual & High Pressure Triple Lumen Acute Catheters	12, 12.5, 13.5	13, 16, 20, 24, 30	Tapered	Dual, triple	Side slots	No	Acute
Medtronic	Mahurkar Pre-Curved Dual Lumen Catheter	11.5	13.5, 16, 19.5, 24	Tapered	Dual	Yes	No	Acute
Medtronic	Mahurkar Pre-Curved Extension Dual Lumen Catheter IC Safety Trays	11.5	13.5, 16, 19.5, 24	Tapered	Dual	Yes	No	Acute
Medtronic	Mahurkar Protection and Safety Solutions (PASS) Trays: Curved Extensions	11.5, 13.5	13.5, 16, 19.5, 24	Tapered	Dual	Yes	No	Acute
Medtronic	Mahurkar Protection and Safety Solutions (PASS) Trays: High Pressure Triple Lumen Catheter-Curved Extension	12	13, 16, 20, 24	Tapered	Triple	Side slots	No	Acute
Medtronic	Mahurkar Protection and Safety Solutions (PASS) Trays: High Pressure Triple Lumen Catheter-Straight Extension	12	20, 24	Tapered	Triple	Side slots	No	Acute
Medtronic	Mahurkar Protection and Safety Solutions (PASS) Trays: Precurved Extensions	13.5	13.5, 16, 19.5, 24	Tapered	Dual	Yes	No	Acute
Medtronic	Mahurkar Protection and Safety Solutions (PASS) Trays: Straight Extensions	11.5, 13.5	13.5, 16, 19.5, 24	Tapered	Dual	Yes	No	Acute
Medtronic	Mahurkar Straight Extension Dual Lumen Catheter	10	12, 15	Tapered	Dual	Yes	No	Acute
Medtronic	Mahurkar Straight Extension Dual Lumen Catheter	11.5	13.5, 16, 19.5, 24	Tapered	Dual	Yes	No	Acute
Medtronic	Mahurkar Straight Extension Dual Lumen Catheter IC Safety Trays	11.5	13.5, 16, 19.5, 24	Tapered	Dual	Yes	No	Acute
Medtronic	Palindrome Precision Heparin Coated and Silver Ion Antimicrobial Dialysis Catheter	14.5	19, 23, 28, 33	Symmetric	Dual	Side slots	Yes, heparin and silver ion antimicrobial	Chronic
Medtronic	Palindrome Precision Heparin Coated Dialysis Catheter	14.5	19, 23, 28, 33	Symmetric	Dual	Side slots	Yes, heparin	Chronic
Medtronic	Palindrome Precision Precurved Symmetric Tip Dual Lumen Catheter	14.5	19, 23, 28, 33	Symmetric	Dual	Side slots	No	Chronic
Medtronic	Palindrome Precision Reverse Tunneled Dialysis Catheter	14.5	19, 23, 28, 33, 44, 55	Symmetric	Dual	Side slots	No	Chronic
Medtronic	Palindrome Precision Silver Ion Antimicrobial Dialysis Catheter	14.5	19, 23, 28, 33	Symmetric	Dual	Side slots	Yes, silver ion antimicrobial	Chronic
Medtronic	Palindrome Precision Symmetric Tip Dual Lumen Catheter	14.5	19, 23, 28, 33, 55	Symmetric	Dual	Side slots	No	Chronic
Medtronic	Permcath Dual Lumen Catheter	Oval-shaped lumen design	13, 19, 23	Staggered	Dual	Yes	No	Chronic

Company Name	Product Name	Type	Position	US FDA Indicated Use
Medtronic	Mo.Ma Ultra Proximal Cerebral Protection Device	Proximal protection	Proximal	Indicated as an EPS to contain and remove embolic material (thrombus/debris) while performing angioplasty and stenting procedures involving lesions of the internal carotid artery and/or the bifurcation; the reference diameter of the external carotid artery should be between 3–6 mm and the reference diameter of the common carotid artery should be between 5–13 mm
Medtronic	SpiderFX Embolic Protection Device	Filter; guidewire of choice	Distal	Lower extremity indication: indicated for use as a guidewire and EPS to contain and remove embolic material in conjunction with the TurboHawk, either during standalone procedures or together with PTA and/or stenting, in the treatment of severely calcified lesions in arteries of the lower extremities; the vessel diameter at the filter basket placement site should be between 3–6 mm; carotid indication: indicated for use as a guidewire and EPS to contain and remove embolic material (thrombus/debris) while performing angioplasty and stenting procedures in carotid arteries; the diameter of the artery at the site of the filter basket placement should be between 3–7 mm; saphenous vein graft indication: indicated for use as an EPS to contain and remove embolic material (thrombus/debris); the device also acts as the guidewire while performing PTCA or stenting procedures in coronary saphenous vein bypass grafts with reference vessel diameters of 3–6 mm

Company Name	Product Name	Technology	Wavelength (nm)	Sheath Sizes (F)	Sheath Lengths (cm)	US FDA Indicated Use
Medtronic	ClosureFast 3 cm Radiofrequency Ablation Catheter	Radiofrequency ablation	Heating length (3 cm); working length of 60 cm	7	7, 11	Intended for endovascular coagulation of blood vessels in patients with superficial venous reflux
Medtronic	ClosureFast 7 cm Radiofrequency Ablation Catheter	Radiofrequency ablation	Heating length (7 cm); working lengths of 60 and 100 cm	7	7, 11	Intended for endovascular coagulation of blood vessels in patients with superficial venous reflux
Medtronic	ClosureFast 8 cm Radiofrequency Ablation Catheter	Radiofrequency ablation	Heating length (8 cm); working lengths of 60 and 100 cm	6	7, 11	Intended for endovascular coagulation of blood vessels in patients with superficial venous reflux
Medtronic	ClosureRFG Endovenous Radiofrequency Generator	Radiofrequency	–	–	–	Intended for use with ClosureFast, ClosureFast 3 cm, and ClosureRFS products
Medtronic	ClosureRFS Endovenous Radiofrequency Stylet	Radiofrequency	–	6 (with 12 cm working length)	–	Intended for use in vessel and tissue coagulation including the treatment of incompetent (ie, refluxing), perforator, and tributary veins
Medtronic	VenaSeal Closure System	Nonthermal, nontumescent (cyanoacrylate-based medical adhesive)	Access with 5-F microintroducer; blue introducer (ID: 5 F, OD: 7 F) included in kit	Access with 5-F microintroducer; blue introducer (ID: 5, OD: 7) included in kit	80, blue introducer included	Indicated for use in the permanent closure of lower extremity superficial truncal veins, such as the great saphenous vein, through endovascular embolization with coaptation; intended for use in adults with clinically symptomatic venous reflux as diagnosed by duplex ultrasound

Company Name	Product Name	Sheath Compatibility (F)	Guidewire Compatibility (inch)	Working Length (cm)	Mode of Operation	US FDA Indicated Use
Medtronic	Liberant Thrombectomy System	6	0.035	135	Mechanical aspiration	Peripheral arterial and venous systems
Medtronic	Liberant Thrombectomy System	8	0.035	50	Mechanical aspiration	Peripheral arterial and venous systems
Medtronic	Liberant Thrombectomy System	8	0.035	115	Mechanical aspiration	Peripheral arterial and venous systems
Medtronic	Liberant Thrombectomy System	12	0.035	115	Mechanical aspiration	Peripheral arterial and venous systems

Company Name	Product Name	Catheter Size/Length (F/cm)	Working Diameters (mm)	Snare Length (cm)	Snare Type	Comments
Medtronic	Alligator Retrieval Device	0.021-inch ID (minimum microcatheter size)	2, 3, 4, 5	175	Retrieval device; 0.016-inch guidewire with four platinum jaws	–
Medtronic	Amplatz GooseNeck Microsnare Kit	2.3–3/150	2, 4, 7	175	Single 90° loop configuration and gold tungsten coils (for enhanced visualization); replacement catheters available in 4 and 6 F 6/102, 15, 20, 25, 30, 35 (48- and 102-cm lengths)	–
Medtronic	Amplatz GooseNeck Microsnare Kit	2.3–3/175	2, 4, 7	200	Single 90° loop configuration and gold tungsten coils (for enhanced visualization); replacement catheters available in 4 and 6 F 6/102, 15, 20, 25, 30, 35 (48- and 102-cm lengths)	–
Medtronic	Amplatz GooseNeck Snare Kit	4/102	5, 10	120	Single 90° loop configuration and gold tungsten coils (for enhanced visualization); replacement catheters available in 4 and 6 F 6/102, 15, 20, 25, 30, 35 (48- and 102-cm lengths)	–
Medtronic	Amplatz GooseNeck Snare Kit	6/102	15, 20, 25, 30, 35	120	Single 90° loop configuration and gold tungsten coils (for enhanced visualization); replacement catheters available in 4 and 6 F 6/102, 15, 20, 25, 30, 35 (48- and 102-cm lengths)	–
Medtronic	Amplatz GooseNeck Snare Kit	4/48, 6/48	10, 25	65	Single 90° loop configuration and gold tungsten coils (for enhanced visualization); replacement catheters available in 4 and 6 F 6/102, 15, 20, 25, 30, 35 (48- and 102-cm lengths)	–

Company Name	Product Name	Type	Maximum Tip Diameter (mm)	Minimum Guide Catheter Size (F)	Catheter Length (cm)
Medtronic	Diver CE Aspiration Catheter	Low-profile, rapid-exchange, hydrophilic coating with and without side holes	1.58	6	145
Medtronic	Export AP Catheter	Full-wall variable hub to tip braiding; hydrophilic coating; short, soft tip	1.73	6	140
Medtronic	React 68 Catheter	Nitinol, coil + braid construction, beveled distal tip	0.068 inch	–	132
Medtronic	Riptide Aspiration System	Aspiration pump, collection canister, intermediate tubing, aspiration tubing	–	–	–
Medtronic	Export Advance	Full-wall variable braiding; preloaded stylet; short, soft tip	1.73	6	140

Company Name	Product Name	Drug Type	Drug Concentration (µg/mm2)	Excipient Type	Guidewire Compatibility (inch)	Shaft Length (cm)	Sheath Compatibility (F)	Balloon Diameters (mm)	Balloon Lengths (mm)	US FDA Indicated Use
Medtronic	In.Pact AV (AVF Indication)	Paclitaxel	3.5	Urea	0.035	40, 80, 130	5 (4 mm), 6 (5, 6 mm), 7 (7–10 mm), 9 (12 mm)	4–12	40, 60, 80, 120	Indicated for PTA, after appropriate vessel preparation, for the treatment of obstructive lesions up to 100 mm in length in the native arteriovenous dialysis fistulae with reference vessel diameters of 4 to 12 mm

Company Name	Product Name	Sheath Compatibility (F)	Guidewire Compatibility (inch)	Working Length (cm)	Mode of Operation	US FDA Indicated Use
Medtronic	Solitaire Platinum Revascularization Device 4 X 20, 4 X 40, 6 X 20	8, 9 (balloon guide)	0.014	180 (Solitaire push wire)	Designed to restore blood flow in patients experiencing ischemic stroke due to large intracranial vessel occlusion and for use in the neurovasculature, such as the internal carotid artery, M1 and M2 segments of the middle cerebral artery, basilar, and the vertebral arteries	Indicated for use to restore blood flow in the neurovasculature by removing thrombus for the treatment of acute ischemic stroke to reduce disability in patients with a persistent, proximal anterior circulation, large vessel occlusion, and smaller core infarcts who have first received IV tPA; endovascular therapy with the device should be started within 6 hours of symptom onset; indicated to restore blood flow by removing thrombus from a large intracranial vessel in patients experiencing ischemic stroke within 8 hours of symptom onset; patients who are ineligible for IV tPA or who fail IV tPA therapy are candidates for treatment
Medtronic	Solitaire X Revascularization Device (4 X 20; 4 X 40; 6 X 20; 6 X 24; 6 X 40 mm)	–	0.021	200	–	(1) Indicated for use to restore blood flow in the neurovasculature by removing thrombus for the treatment of acute ischemic stroke to reduce disability in patients with a persistent, proximal anterior circulation, large vessel occlusion, and smaller core infarcts who have first received intravenous tissue plasminogen activator (IV t-PA)—endovascular therapy with the device should be started within 6 hours of symptom onset; (2) indicated to restore blood flow by removing thrombus from a large intracranial vessel in patients experiencing ischemic stroke within 8 hours of symptom onset—patients who are ineligible for IV t-PA or who fail IV t-PA therapy are candidates for treatment; (3) indicated for use to restore blood flow in the neurovasculature by removing thrombus for the treatment of acute ischemic stroke to reduce disability in patients with a persistent, proximal anterior circulation, large vessel occlusion of the internal carotid artery (ICA) or middle cerebral artery (MCA)-M1 segments with smaller core infarcts (< 70 mL by CTA or MRA; < 25 mL by MR-DWI)—endovascular therapy with the device should start within 6–16 hours of time last seen well in patients who are ineligible for IV t-PA or who fail IV t-PA therapy
Medtronic	Solitaire X-Pack (2 pack: 4 X 40 or 6 X 40 mm with Phenom 21 or 27)	–	–	200	–	(1) Indicated for use to restore blood flow in the neurovasculature by removing thrombus for the treatment of acute ischemic stroke to reduce disability in patients with a persistent, proximal anterior circulation, large vessel occlusion, and smaller core infarcts who have first received intravenous tissue plasminogen activator (IV t-PA)—endovascular therapy with the device should be started within 6 hours of symptom onset; (2) indicated to restore blood flow by removing thrombus from a large intracranial vessel in patients experiencing ischemic stroke within 8 hours of symptom onset—patients who are ineligible for IV t-PA or who fail IV t-PA therapy are candidates for treatment; (3) indicated for use to restore blood flow in the neurovasculature by removing thrombus for the treatment of acute ischemic stroke to reduce disability in patients with a persistent, proximal anterior circulation, large vessel occlusion of the internal carotid artery (ICA) or middle cerebral artery (MCA)-M1 segments with smaller core infarcts (< 70 mL by CTA or MRA; < 25 mL by MR-DWI)—endovascular therapy with the device should start within 6–16 hours of time last seen well in patients who are ineligible for IV t-PA or who fail IV t-PA therapy
Medtronic	Solitaire X-Pack (3 pack: 4 X 40 or 6 X 40 mm with Phenom 21 or 27 or React 68 or 71)	–	–	200	–	(1) Indicated for use to restore blood flow in the neurovasculature by removing thrombus for the treatment of acute ischemic stroke to reduce disability in patients with a persistent, proximal anterior circulation, large vessel occlusion, and smaller core infarcts who have first received intravenous tissue plasminogen activator (IV t-PA)—endovascular therapy with the device should be started within 6 hours of symptom onset; (2) indicated to restore blood flow by removing thrombus from a large intracranial vessel in patients experiencing ischemic stroke within 8 hours of symptom onset—patients who are ineligible for IV t-PA or who fail IV t-PA therapy are candidates for treatment; (3) indicated for use to restore blood flow in the neurovasculature by removing thrombus for the treatment of acute ischemic stroke to reduce disability in patients with a persistent, proximal anterior circulation, large vessel occlusion of the internal carotid artery (ICA) or middle cerebral artery (MCA)-M1 segments with smaller core infarcts (< 70 mL by CTA or MRA; < 25 mL by MR-DWI)—endovascular therapy with the device should start within 6–16 hours of time last seen well in patients who are ineligible for IV t-PA or who fail IV t-PA therapy

Company Name	Product Name	Size (F)	Recommended Introducer Size (F)	Guidewire Compatibility (inch)	Catheter Length (cm)	Maximum Inflated Balloon Diameter (mm)
Medtronic	Reliant Stent Graft Balloon Catheter	8	12	0.038 or smaller	100	46

Company Name	Product Name	Size (F)	Guidewire Compatibility (inch)	Comments
Medtronic	Sentrant Introducer Sheath With Hydrophilic Coating	12–26	0.035	Hemostatic and kink-resistant introducer sheath
Medtronic	TourGuide Steerable Sheath With Hydrophobic Coating	6.5, 7, 8.5	0.035, 0.038	Steerable hydrophobic coating, self-locking rotating knob, and wide variety of applications within the human vasculature, from the periphery to the intracardiac

Company Name	Product Name	Stent Material	Graft Material	Stent Expansion	Length (cm)	Diameter (mm)	Sheath Required for Delivery	Sheath Compatibility (F)
Medtronic	Valiant Thoracic Stent Graft on Captivia Delivery System	Nitinol	Woven polyester	Self expanding	10, 15, 20	22, 24, 26, 28, 30, 32, 34, 36, 38, 40, 42, 44, 46; tapered: 26, 28, 30, 32, 34, 36, 38, 40, 42, 44, 46	No	22, 24, 25 (OD)

Company Name	Product Name	Size (F)	Recommended Introducer Size (F)	Guidewire Compatibility (inch)	Catheter Length (cm)	Maximum Inflated Balloon Diameter (mm)
Medtronic	Reliant Stent Graft Balloon Catheter	8	12	0.038 or smaller	100	46

Company Name	Product Name	Size (F)	Guidewire Compatibility (inch)	Comments
Medtronic	Sentrant Introducer Sheath With Hydrophilic Coating	12–26 (sheath)	0.035	Hemostatic and kink-resistant introducer sheath

Company Name	Product Name	Type of Catheter Construction	Proximal Size (F)	Middle Size (F)	Distal Size (F)	Catheter Working Length (cm)	Catheter Endhole Diameter ID (inch)	Recommended Guidewire Size (inch)	Radiopaque Tip (Yes/No)	Hydrophilic Coating (Yes/No)
Medtronic	Apollo Onyx Delivery Micro Catheter	–	2.7	–	1.5	165	0.013	0.010	Yes	Yes
Medtronic	Echelon 10 Micro Catheter	–	2.1	–	1.7	150	0.017	0.014	Yes	Yes
Medtronic	Echelon 14 Micro Catheter	–	2.4	–	1.9	150	0.017	0.014	Yes	Yes
Medtronic	Marathon Flow Directed Micro Catheter	–	2.7	–	1.5	165	0.013	0.010	Yes	Yes
Medtronic	Marksman Micro Catheter	–	3.2	–	2.8	105, 135, 150, 160	0.027	0.021	Yes	Yes
Medtronic	Orion Micro Catheter	–	2.4	–	2.6	150	0.021	0.018	Yes	Yes
Medtronic	Rebar 10 Reinforced Micro Catheter	–	2.3	–	1.7	153	0.015	0.012	Yes	Yes
Medtronic	Rebar 14 Reinforced Micro Catheter	–	2.4	–	1.9	153	0.017	0.014	Yes	Yes
Medtronic	Rebar 18 Reinforced Micro Catheter	–	2.7	–	2.4	130, 153	0.021	0.018	Yes	Yes
Medtronic	Rebar 27 Reinforced Micro Catheter	–	2.8	–	2.8	130	0.027	0.021	Yes	Yes
Medtronic	UltraFlow HPC Micro Catheter	–	3	–	1.9	165	0.012	0.010	Yes	Yes

Company Name	Product Name	Sheath Compatibility (F)	Guidewire Compatibility (inch)	Working Length (cm)	Mode of Operation	US FDA Indicated Use
Medtronic	Cragg-McNamara Valved Infusion Catheter	4, 5	0.035, 0.038	40, 65, 100, 135	Catheters with radiopaque markers proximal and distal to the infusion segments; Cragg-MicroValve at the distal tip provides endhole occlusion	Indicated for use in the controlled selective infusion of physician-specific pharmacological agents or radiopaque contrast media in the general vasculature

Company Name	Product Name	Modality	Recommended Vessel Size (mm)	Number of Catheter Sizes	Balloon Diameter (mm)	Wire Compatibility (inch)	Catheter Size (F)	Catheter Length (cm)	Guide Catheter Compatibility (F)	Safety Mechanisms	US FDA Indicated Use
Medtronic	Symplicity Spyral	Radiofrequency	Renal arteries 3–8 mm in diameter	One	–	0.014	4	117	6	Integrated into generator; algorithm to monitor temperature and impedance followed by active power modulation to prevent non-target tissue damage	Indicated to reduce blood pressure as an adjunctive treatment in patients with hypertension in whom lifestyle modifications and antihypertensive medications do not adequately control blood pressure