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Medtronic Receives CE Marking for its 31mm CoreValve Percutaneous Aortic Valve

August 22nd, 2011 Gavin Corley Cardiac Surgery, Cardiology, Radiology

Medtronic has received CE marking for the latest addition to its CoreValve family of transcatheter aortic valves. The CoreValve System has been designed to provide a minimally invasive treatment option for patients with symptomatic, severe aortic stenosis who are at high risk, or are ineligible, for open-heart surgery.

According to the press release, the new 31mm CoreValve system is the largest transcatheter valve available and can be deployed through the same delivery system as smaller CoreValve sizes. Individual valve sizing is essential for achieving ideal patient blood flow and for minimizing the risk of adverse events.

Medtronic’s CoreValve family now includes 26mm, 29mm and 31mm valve sizes – all based on the self-expanding platform that was CE marked in 2007. To date CoreValve System has been implanted in over 15,000 patients in more than 40 countries. The CoreValve System is currently limited to investigational use in the United States.

Press release: Medtronic Gains CE Mark for 31mm CoreValve® Percutaneous Aortic Valve …

Product page: The CoreValve System …

Previous coverage of CoreValve at Medgadget…

Gavin Corley

Gavin holds a first-class Bachelor’s degree in Electronic Engineering degree from the University of Limerick and a Ph.D. in Biomedical Engineering from the National University of Ireland, Galway. He is currently a post-doctoral research and project leader at the NUI Galway where he has spent the last 2 years leading the product development and commercialization of two novel technologies for the management of varicose veins and chronic venous leg ulcers. He has published several research papers in the fields of anatomy, physiology and medical physics and is the lead author of one patent application to date. In his free time Gavin has been known to swim, cycle and hum a tune or two.

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