Home » IDEV TECHNOLOGIES GAINS A 510(K) CLEARANCE FOR ITS INTERWOVEN NITINOL SELF-EXPANDING STENT: SUPERA
IDEV TECHNOLOGIES GAINS A 510(K) CLEARANCE FOR ITS INTERWOVEN NITINOL SELF-EXPANDING STENT: SUPERA
August 29, 2006
IDEV Technologies, Inc., an emerging leader in the development and marketing of minimally invasive stent technologies, announced that the company received a 510(k) clearance from FDA for the first interwoven nitinol self-expanding stent available in the United States. The newly approved SureSave Stent will be renamed SUPERA(TM).
Genetic Engineering News (http://www.genengnews.com/news/bnitem.aspx?name=5170612)
KEYWORDS FDAnews Device Daily Bulletin
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