510(k) K202232 ยท PHX Shoulder Prosthesis, Reverse Configuration
Comprehensive Vault Reconstruction System
| Applicant | Biomet Manufacturing Corp, Warsaw IN, US |
| Decision | Substantially Equivalent, Feb 19, 2021 |
| Received | Aug 7, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K202232
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.