FDA 510(k) Applications Submitted by Stryker Corporation (Tornier, S.A.S.)
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K241491 | 05/24/2024 | Blueprint Patient-Specific Instrumentation; Shoulder iD Primary Reversed Glenoid | Stryker Corporation (Tornier, S.A.S.) |
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