510(k) K234105 ยท PHX Shoulder Prosthesis, Reverse Configuration
Catalyst F1x Shoulder System
| Applicant | Catalyst Orthoscience, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Apr 5, 2024 |
| Received | Dec 26, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K234105
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.