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AMDS Hybrid Prosthesis ("AMDS")

Artivion, Inc. · Model K039420 · UDI-DI 00877234001192

QSK Prescription
0
510(k) clearances
331
Adverse events (34 deaths)
0
Recalls
4
Facilities

Description

40mm Straight Stent (24mm collar)

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.