510(k) K211074 ยท PHX Shoulder Prosthesis, Reverse Configuration
Univers Revers Modular Glenoid System, Standard Augment Baseplates
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Sep 2, 2021 |
| Received | Apr 12, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K211074
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.