Tornier S.A.S.
FDA 510(k) & PMA Approved Devices — 10 products
Total Devices10
Categories5
Latest Approval2024-02-21
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K232265 | BLUEPRINT Patient Specific Instrumentation | PHX | 2024-02-21 | View |
| 510(k) | K222510 | Blueprint Mixed Reality system | OLO | 2023-01-20 | View |
| 510(k) | DEN220012 | Tornier Pyrocarbon Humeral Head | QKW | 2022-12-16 | View |
| 510(k) | K203315 | BLUEPRINT Patient Specific Instrumentation | KWS | 2021-04-15 | View |
| 510(k) | K190521 | Aequalis Ascend Flex Shoulder System | KWS | 2019-06-12 | View |
| 510(k) | K162800 | BLUEPRINT Patient Specific Instrumentation | KWS | 2017-02-22 | View |
| 510(k) | K161789 | BLUEPRINT Patient Specific Instrumentation | KWS | 2016-12-27 | View |
| 510(k) | K153452 | Salto XT, Salto Talaris | HSN | 2016-08-11 | View |
| 510(k) | K160555 | BLUEPRINT Patient Specific Instrumentation | KWS | 2016-06-10 | View |
| 510(k) | K152966 | Aequalis Fx2 | PHX | 2016-01-14 | View |
No matching devices.