October 5, 2015 — The U.S. Food and Drug Administration (FDA) has approved Boston Scientific’s Synergy Bioabsorbable Polymer Drug-Eluting Stent System (BP-DES) for the treatment of coronary artery disease. This is the first stent approved on the U.S. market that uses a metallic stent with a bioresorbable polymer drug-carrier rather than permanent polymers, which have been implicated as a cause of late-stent thrombosis.Â
