510(k) K211729 · PHX Shoulder Prosthesis, Reverse Configuration
Comprehensive® Convertible Glenoid - Vivacit-E Liner
| Applicant | Biomet Manufacturing Corp, Warsaw IN, US |
| Decision | Substantially Equivalent, Nov 4, 2021 |
| Received | Jun 4, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K211729
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.