Stryker Corporation (Tornier, S.A.S.)
2 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| Blueprint Patient-Specific Instrumentation (K253674) | Stryker Corporation (Tornier, S.A.S.) | 2026-04-03 |
| Blueprint Patient-Specific Instrumentation; Shoulder iD Primary Reversed Glenoid (K241491) | Stryker Corporation (Tornier, S.A.S.) | 2024-10-10 |
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Every clearance here is in the API, with alerts when new ones post.