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Absorbable Coronary Drug-Eluting Stent

FDA product code PNY · Class 3 · Unknown

14
Registered devices
929
Adverse events
1
Recalls
0
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2017-04-26Abbott VascularAbbott Vascular is initiating a recall of the Absorb Bioresorbable Vascular Scaffold (BVS) System due to studies showing elevated rates of major adverse events,

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.