510(k) K223801 ยท PHX Shoulder Prosthesis, Reverse Configuration
FX V135(TM) Shoulder Prosthesis
| Applicant | Fx Shoulder USA, Inc., Dallas TX, US |
| Decision | Substantially Equivalent, Jun 5, 2023 |
| Received | Dec 19, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223801
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.