510(k) K233482 · PHX Shoulder Prosthesis, Reverse Configuration
Equinoxe® Central Screw Baseplate System
| Applicant | Exactech, Inc., Gainesville FL, US |
| Decision | Substantially Equivalent, Jul 18, 2024 |
| Received | Oct 26, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233482
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.