510(k) K131353 ยท PHX Shoulder Prosthesis, Reverse Configuration
COMPREHENSIVE REVERSE SHOULDER - TITANIUM GLENOSPHERE
| Applicant | Biomet Manufacturing Corp, Warsaw IN, US |
| Decision | Substantially Equivalent, Oct 8, 2013 |
| Received | May 10, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131353
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.