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DYNAFIX VS OSTEOTOMY SYSTEM
Biomet Orthopedics, LLC · Model 14065P · UDI-DI 00887868090141
1
510(k) clearances
8
Adverse events
1
Recalls
10
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2013-10-11 | Zimmer, Inc. | Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. (ZMBV) facility in Ponce, Puerto Rico. Based on this review, it was determ |
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Get your free API keyRead the docsData 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.