510(k) K210790 ยท PHX Shoulder Prosthesis, Reverse Configuration
Lateralized and Augmented Baseplates
| Applicant | Fx Shoulder USA, Inc., Dallas TX, US |
| Decision | Substantially Equivalent, Aug 25, 2021 |
| Received | Mar 16, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K210790
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.