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INFUSE® Bone Graft

MEDTRONIC SOFAMOR DANEK, INC. · Model 7510600 · UDI-DI 00681490843812

NPZNEK Prescription
0
510(k) clearances
235
Adverse events
1
Recalls
6
Facilities

Description

BONE GRAFT KIT 7510600 INFUSE LARGE

Recalls

DateFirmReason
2005-02-17Dentsply Friadent CeramedPepGen P-15 Putty kit was labeled with the incorrect expiration date.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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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.