2014 Buyer’s Guide

This Buyer’s Guide offers a searchable, comprehensive listing of the FDA-approved interventional devices available in the United States.

 
 

News

 

Codman Neuro Launches 7-F Envoy DA XB Guiding Catheter

July 30, 2014—Codman Neuro, part of DePuy Synthes Companies of Johnson & Johnson, announced the launch of the Envoy DA XB distal access guiding catheter and the 7-F …

FDA Clears Teleflex’s 150-cm Arrow GPS Balloon Dilatation Catheter

July 29, 2014—Teleflex Incorporated announced that its subsidiary Hotspur Technologies, Inc. received US Food and Drug Administration 510(k) clearance to market the Arro…

Boston Scientific Launches Polaris Imaging System

July 22, 2014—Boston Scientific Corporation announced the full commercial launch of the Polaris imaging system that will support the company’s family of intravascu…

Spectranetics Announces FDA Clearance of Peripheral Laser Atherectomy Devices for In-Stent Restenosis

July 23, 2014—Spectranetics Corporation announced that it has received US Food and Drug Administration (FDA) clearance of its Turbo-Tandem and Turbo Elite peripheral ath…

Biotronik Completes Enrollment in SFA Arm of the BIOFLEX-I Study

July 22, 2014—Biotronik announced the completion of patient enrollment in the superficial femoral artery (SFA) arm of the company’s BIOFLEX-I clinical trial, …

Teleflex’s Arrow-Clark VectorFlow Chronic Hemodialysis Catheter Receives FDA Clearance

July 22, 2014—Teleflex Incorporated announced that it has received 510(k) clearance from the US Food and Drug Administration to market its Arrow-Clark VectorFlow chronic…

SCAI Publishes Expert Consensus Recommendations for Treating Below-the-Knee PAD

July 18, 2014—The Society for Cardiovascular Angiography and Interventions (SCAI) announced the publication of expert consensus recommendations, “SCAI Expert …

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I Object! Questions Facing Physicians’ Rights to Dispute Sunshine Data

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Invention and Intellectual Property

Protecting Your Inventions, From Idea to Marketplace

The first step in bringing your medical device to market is to understand who owns the rights to your invention.

Beginning the Patent Process

The second step in bringing your medical device to market is to understand whether you can protect your invention.

Evaluating Freedom to Operate

The third step in bringing your medical device to market is to understand whether you can practice your invention.

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About Endovascular Today

Endovascular Today is a publication dedicated to bringing you comprehensive coverage of all the latest technology, techniques, and developments in the endovascular field. Our Editorial Advisory Board is composed of the top endovascular specialists, including interventional cardiologists, interventional radiologists, vascular surgeons, neurologists, and vascular medicine practitioners, and our publication is read by an audience of more than 22,000 members of the endovascular community.

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