Two-year Clinical Data Demonstrate Low Adverse Event Rates, Including No Myocardial Infarction or Stent Thrombosis, for the Boston Scientific 2.25 mm PROMUS Element Platinum Chromium Stent NATICK, ...
Gaithersburg, MD - Seven months after an FDA advisory panel voted nine to one to recommend approval of the Xience V everolimus-eluting stent (Abbott Vascular), the FDA has granted marketing approval ...
NATICK, Mass., Feb. 12, 2013 -- Boston Scientific Corporation (NYSE: BSX) has received CE Mark approval for the Promus PREMIER™ Everolimus-Eluting Platinum Chromium Coronary Stent System, the ...
November 24, 2011 (Rockville, Maryland and Detroit, Michigan) — The US Food and Drug Administration (FDA) has approved the Promus Element Plus everolimus-eluting chromium platinum coronary stent ...
12-month clinical data demonstrate low adverse event rates for Boston Scientific's 2.25 mm PROMUS Element Platinum Chromium Stent NATICK, Mass. and PARIS, Boston Scientific Corporation today announced ...
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