510(k) K223655 ยท PHX Shoulder Prosthesis, Reverse Configuration
Catalyst R1 Reverse Shoulder System
| Applicant | Catalyst Orthoscience, Inc., Naples FL, US |
| Decision | Substantially Equivalent, May 9, 2023 |
| Received | Dec 6, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223655
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.