510(k) K212415 ยท PHX Shoulder Prosthesis, Reverse Configuration
Arthrex Modular Glenoid System-Titanium Glenosphere
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Nov 17, 2021 |
| Received | Aug 3, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212415
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.