Overture Resurfacing, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest Approval2023-07-07
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K231253 | Overture Orthopaedics Patellofemoral System | KRR | 2023-07-07 | View |
| 510(k) | K221292 | Uni Knee Resurfacing System | HSX | 2023-03-10 | View |
No matching devices.