510(k) K232265 · PHX Shoulder Prosthesis, Reverse Configuration
BLUEPRINT Patient Specific Instrumentation
| Applicant | Tornier S.A.S., Montbonnot-Saint-Martin, FR |
| Decision | Substantially Equivalent, Feb 21, 2024 |
| Received | Jul 31, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K232265
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.