From Abbot Medical: Once again, Abbott is leading the wave of innovation in stent technology. The XIENCE V Drug Eluting Stent's proven design combines the deliverability of MULTI-LINK VISION with a biocompatible fluorinated copolymer and everolimus to assist in increased treatment success for patients with coronary artery disease (CAD).
Abbott announced that FDA approved the XIENCE V Everolimus Eluting Coronary Stent System for the treatment of coronary artery 
The Xience represents the fourth Drug Eluting Stent approved following the Cypher and Taxus from J&J and Boston Scientific respectively. Earlier this year the Endeavor was released from Medtronic. Interestingly, as a consequence of the original Guidant buyout deal, two identical stents will be released. The Promus from Boston Scientific and the Xience from Abbott
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