510(k) K231911 · PHX Shoulder Prosthesis, Reverse Configuration
Glenoid Reconstruction System Full Wedge Baseplate
| Applicant | Medacta International S.A., Castel San Pietro (Ch), CH |
| Decision | Substantially Equivalent, Nov 9, 2023 |
| Received | Jun 29, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231911
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.