Stryker Corporation (Tornier, Inc.)
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories2
Latest FDA decision2026-06-12
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K260102 | Tornier Perform Reversed Glenoid and Tornier Perform Reversed Augmented Glenoid Shoulder System | PHX | 2026-06-12 | View |
| 510(k) | K241878 | Tornier Humeral Reconstruction System (Tornier HRS); Tornier Perform Humeral System - Stem (Tornier PHS-Stem) | KWS | 2024-12-06 | View |
| 510(k) | K241609 | Tornier Humeral Reconstruction System (Tornier HRS) | KWS | 2024-09-10 | View |
No matching devices.