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INFUSE® Bone Graft

MEDTRONIC SOFAMOR DANEK, INC. · Model 7510800 · UDI-DI 00681490843829

MPWNEKNPZ Prescription
0
510(k) clearances
74
Adverse events (1 deaths)
1
Recalls
2
Facilities

Description

BONE GRAFT KIT 7510800 INFUSE LARGE II

Recalls

DateFirmReason
2008-06-24Stryker BiotechProduct Package Insert misprint-text offset

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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.