510(k) K240278 ยท PHX Shoulder Prosthesis, Reverse Configuration
Full Wedge Lateralized and Augmented Baseplates
| Applicant | Fx Shoulder USA, Inc., Addison TX, US |
| Decision | Substantially Equivalent, May 15, 2024 |
| Received | Feb 1, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K240278
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.