FDA To Review Abbott's XIENCE Drug Eluting Heart Stent

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Abbott to Present Comprehensive Safety and Efficacy Data on XIENCE V Drug Eluting Heart Stent to FDA Advisory Committee on November 29


Data in Pre-Market Approval Application Are First Ever to Demonstrate Superiority of One Drug Eluting Stent Over Another in a Randomized Controlled Clinical Trial

New Data Released Confirms Consistency of Results for Late Loss, TVF, MACE, TLR, Cardiac Death, MI, Thrombosis Across all XIENCE V Studies

Abbott today released a summary of clinical highlights on the XIENCE


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