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EVToday EVToday + CIToday

evt | Article | October 2025

Identifying the Right Carotid Therapy for Each Patient

Dr. William Gray talks with Drs. Sonya Noor, Adnan Siddiqui, and Peter Soukas about how they approach treatment decisions for patients with carotid artery disease, their algorithms, patient and lesion characteristics that help guide decisions, and their shared decision-making process with both the multidisciplinary team and individual patient.

With moderator William A. Gray, MD, MSCAI, FACC, and panelists Sonya Noor, MD, FACS; Adnan Siddiqui, MD, PhD; and Peter A. Soukas, MD

evt | Article | October 2005

Patient-Specific Anatomy in Interventional Vascular Simulation

Already an invaluable training tool, actual patient-specific modules will soon make simulators even more effective.

By William Gray, MD, and Giora Weisz, MD

evt | Article | September 2019

Panel Discussion: Exploring the Paclitaxel Safety Signal

Experts discuss considerations in trial design, adjudication, and paths forward.

With Marianne Brodmann, MD; William Gray, MD; Peter A. Schneider, MD; Ramon L. Varcoe, MBBS, MS, FRACS, PhD; and Thomas Zeller, MD, PhD

evt | News | March 5, 2018

LIBERTY 360° Study's 18-Month Outcomes Presented for CSI's Orbital Atherectomy System

March 6, 2018—Cardiovascular Systems, Inc. (CSI) announced that 18-month outcomes from its LIBERTY 360° study were presented by William Gray, MD, at CRT 2018, the Cardiovascular Research Technologies conference held March 3–6 in Washington, DC.

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evt | News | February 6, 2017

Six-Month Data Presented From CSI's LIBERTY 360° Study of Treatment for Lower Extremity PAD

February 6, 2017—Cardiovascular Systems, Inc. (CSI) announced that 6-month data from the LIBERTY 360° study were presented by William Gray, MD, at ISET 2017, the 29th International Symposium on Endovascular Therapy in Hollywood, Florida.

evt | News | November 6, 2018

Data From the TOBA II Trial Presented for Intact's Tack Endovascular System

November 6, 2018—Intact Vascular, Inc. announced that the company's Tack Optimized Balloon Angioplasty II (TOBA II) clinical trial of the Tack endovascular system achieved both primary and secondary endpoints.

evt | News | April 20, 2021

Philips Stellarex DCB’s Safety Profile at 5 Years Confirmed by Meta-Analysis

April 20, 2021—Royal Philips announced that findings from a 5-year patient-level meta-analysis of two major randomized controlled trials (RCTs) of the Stellarex low-dose paclitaxel drug-coated balloon (DCB) were presented by William Gray, MD, at the 2021 Charing Cross International Symposium, which was held virtually.

evt | News | April 20, 2010

Iliac Indication Approved for Medtronic's Complete SE

April 21, 2010—Medtronic, Inc. (Minneapolis, MN) announced that it has received approval from the US Food and Drug Administration (FDA) for the Complete SE self-expanding vascular stent system to be used for treating peripheral artery disease (PAD) in the iliac arteries.

evt | News | April 20, 2010

FDA Approves Iliac Indication for Medtronic's Complete SE Stent

April 21, 2010—Medtronic, Inc. (Minneapolis, MN) announced that it has received approval from the US Food and Drug Administration (FDA) for the Complete SE self-expanding vascular stent system to be used for treating peripheral artery disease (PAD) in the iliac arteries.

evt | News | September 11, 2013

Enrollment Begins in SCAFFOLD Study for Gore Carotid Stent

September 12, 2013—Gore & Associates (Flagstaff, AZ) announced commencement of enrollment in SCAFFOLD, the Gore Carotid Stent Clinical Study for the Treatment of Carotid Artery Stenosis in Patients at Increased Risk for Adverse Events from Carotid Endarterectomy.

evt | News | August 27, 2019

Enrollment Completed in Pivotal TRANSCEND Clinical Trial for Surmodics' SurVeil DCB

August 28, 2019—Surmodics, Inc. announced that it has completed enrollment in the TRANSCEND pivotal clinical trial for the company's SurVeil drug-coated balloon (DCB).

evt | Article | October 2005

Medical Simulation

An overview of the history, current state, and future applications of this promising training tool.

evt | News | February 23, 2012

Roll-In Data From Lombard Medical's PYTHAGORAS AAA Trial Presented

February 24, 2012—Data from the roll-in phase of the PYTHAGORAS trial evaluating abdominal aortic aneurysm (AAA) repair using the Aorfix endovascular stent graft (Lombard Medical Technologies, Inc., Tempe, AZ) were presented at the VEITH Symposium in New York City in November and at the International Symposium on Endovascular Therapy in Miami Beach in January.Thirty-day and 1-year follow-up data from the roll-in phase demonstrated no cases of the graft failing to seal against the artery wall; no cases of graft leakage, migration, or fracture; and, in all cases, the aneurysm sac decreased in diameter or remained stable after implantation of the Aorfix.

evt | News | June 26, 2020

ILLUMENATE EU RCT Results Evaluate Philips’ Stellarex DCB at 4 Years

June 26, 2020—Royal Philips announced 4-year results from the ILLUMENATE European Randomized Controlled Trial (EU RCT) evaluating the safety and efficacy of Philips’ Stellarex 0.035-inch low-dose drug-coated balloon (DCB) to restore and maintain patency in the superficial femoral artery and popliteal arteries of patients with peripheral artery disease (PAD).

Sponsored by Medtronic

evt | Article | November 2023

Roundtable Discussion: Paclitaxel Safety and What We Have Learned

With William A. Gray, MD; Sahil A. Parikh, MD; and Peter A. Schneider, MD

evt | News | May 2, 2023

Vivasure Commences Pivotal PATCH Study of PerQseal Closure Device System

May 2, 2023—Vivasure Medical, an Ireland-based company developing fully absorbable technology for percutaneous vessel closure, announced it has commenced the company’s PATCH pivotal study, which is evaluating the safety and efficacy of the Vivasure PerQseal closure device system.

evt | News | November 20, 2017

Cagent Vascular's Serrantor Alto PTA Serration Balloon Catheter Receives CE Mark

November 21, 2017—Cagent Vascular announced that its Serranator Alto PTA serration balloon catheter has received CE Mark approval.

evt | News | November 14, 2022

Contego’s Neuroguard IEP PERFORMANCE II Carotid Stent Trial Completes Enrollment

November 14, 2022—Contego Medical, Inc. announced that enrollment of the PERFORMANCE II clinical trial has been completed.

evt | News | November 2, 2016

Global DISRUPT PAD III Trial Will Evaluate Shockwave Medical's Lithoplasty System Combined With DCB Therapy in Calcified PAD

November 1, 2016—Shockwave Medical announced plans for the DISRUPT PAD III multicenter randomized trial that will exclusively enroll patients with calcified peripheral artery disease (PAD) to assess short- and long-term outcomes of the company’s Lithoplasty system in combination with drug-coated balloon (DCB) therapy compared to traditional percutaneous transluminal balloon angioplasty (PTA) before DCB treatment in a calcified patient population.

evt | News | October 15, 2024

Contego Medical’s Neuroguard IEP System Approved by FDA for Carotid Revascularization

October 15, 2024—Contego Medical announced FDA premarket approval of the company’s Neuroguard IEP system.


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Carotid Coding Dialysis Embolization EVAR HTN Limb Salvage Neurointervention Oncology Radial Regulatory Renal SFA TEVAR Venous
Centers

Carotid Coding Dialysis Embolization EVAR HTN Limb Salvage Neurointervention Oncology Radial Regulatory Renal SFA TEVAR Venous

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Endovascular Today (ISSN 1551-1944 print and ISSN 2689-792X online) is a publication dedicated to bringing you comprehensive coverage of all the latest technology, techniques, and developments in the endovascular field.



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