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Filler, Recombinant Human Bone Morphogenetic Protein, Collagen Scaffold, Osteoinduction

FDA product code MPW · Class 3 · Unknown

1
Registered devices
74
Adverse events
1
Recalls
0
510(k) clearances

Devices with this code

INFUSE® Bone Graft — MEDTRONIC SOFAMOR DANEK, INC.

Recent recalls

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

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

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