Zimmer Biomet
FDA 510(k) & PMA Approved Devices — 5 products
Total Devices5
Categories5
Latest FDA decision2025-08-15
SEC Filings: 1 filings on record. Latest: 8-K (2026-08-05). View on SEC EDGAR →
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K251834 | Persona Partial Knee | HSX | 2025-08-15 | View |
| 510(k) | K243571 | Trabecular Metal Acetabular Revision System, Acetabular Liners and Constrained Liners | JDI | 2025-07-31 | View |
| 510(k) | K251620 | A.L.P.S. Proximal Humerus Plating System | HRS | 2025-07-25 | View |
| 510(k) | K250834 | Zimmer Biomet Ceramic Heads (22.2mm diameter) | LZO | 2025-04-18 | View |
| 510(k) | K243293 | Zimmer® Persona® Personalized Knee System | MBH | 2024-12-20 | View |
No matching devices.
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