510(k) K241491 ยท PHX Shoulder Prosthesis, Reverse Configuration
Blueprint Patient-Specific Instrumentation; Shoulder iD Primary Reversed Glenoid
| Applicant | Stryker Corporation (Tornier, S.A.S.), Montbonnot-Saint-Martin, FR |
| Decision | Substantially Equivalent, Oct 10, 2024 |
| Received | May 24, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241491
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.