Home › Device types › OJZ
Filler, Recombinant Human Bone Morphogenetic Protein, Collagen Scaffold, Osteoinduction - Hde
FDA product code OJZ · Class f · Unknown
0
Registered devices
1
Adverse events
1
Recalls
0
510(k) clearances
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2010-10-25 | Stryker Biotech | A change to the Preparation for Use section was identified where 2.5cc was replaced with 2cc-3cc volume and was not approved |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.