510(k) K253674 ยท PHX Shoulder Prosthesis, Reverse Configuration
Blueprint Patient-Specific Instrumentation
| Applicant | Stryker Corporation (Tornier, S.A.S.), Montbonnot-Saint-Martin, FR |
| Decision | Substantially Equivalent, Apr 3, 2026 |
| Received | Nov 21, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K253674
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.