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March 18, 2024

Baylis Launches PowerWire Pro RF Guidewire

March 18, 2024—Baylis Medical Technologies Inc. announced FDA 510(k) clearance of the PowerWire Pro radiofrequency (RF) guidewire for facilitating venous stent recanalization for total occlusions. The company advised it has launched the device in the United States.

According to the company, the PowerWire Pro RF guidewire is designed to address the challenge of reocclusion by employing RF technology to cross totally occluded stents in peripheral vessels. The device allows selective application of RF energy to cross segments of the occlusion that cannot be traversed mechanically. When contacting metal, the RF energy terminates, reducing the potential for vessel extravasation when crossing in-stent occlusions.

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March 19, 2024

Medtronic’s Symplicity Spyral RDN System Receives Health Canada License

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March 18, 2024

Biotronik’s Freesolve BTK RMS for CLTI Granted FDA Breakthrough Device Designation

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