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One-Year European Registry Data Released for Popliteal Stenting With SUPERA®
Date:2/8/2011

w SUPERA is uniquely suited to the femoropopliteal anatomy, indicating it may indeed be a market-changing technology."

D. Christopher Metzger, M.D. is the Director of Cardiac and Peripheral Labs and Medical Director of Clinical Research at Wellmont CVA Heart Institute.  He is an investigator in the SUPERB trial, and also on faculty at LINC.  He remarked, "This data correlates well with our own experience with the SUPERA stent.  I believe we can now confidently stent, knowing that SUPERA will remain physiologically conformable, will not fracture, and will have excellent long-term patency.  In my opinion, future trials will confirm that the SUPERA stent will be an excellent front-line therapy for a majority of infra-inguinal endovascular interventions, especially in areas that have typically been a 'no-stent' zone."

Independent mechanical testing reported zero stent fractures for any SUPERA stent assessed after 10 million cycles of 120 degrees flexion and extension and 20 million cycles of torsion.  In comparison, all standard nitinol stents tested fractured before 100,000 cycles in the flexion and extension testing and before 1 million cycles in compression load testing.  The SUPERA stent was demonstrated to have a minimum of four times the radial strength and 360 percent stronger crush resistance than standard nitinol stents, and completely resisted fracturing, kinking, crushing, and crimping.

"The data from the Leipzig popliteal registry is very promising," observed Christopher Owens, President and CEO of IDEV.  "We are very excited about the feedback we are receiving from physicians who have direct experience with the SUPERA stent.  The fact that no other stent has been evaluated in the popliteal artery, let alone shown this level of patency, gives us confidence that it's truly a unique device in a growing market."

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