510(k) K140652 ยท PHX Shoulder Prosthesis, Reverse Configuration
POROUS COATED COMPREHENSIVE FRACTURE STEMS
| Applicant | Biomet Manufacturing Corp, Warsaw IN, US |
| Decision | Substantially Equivalent, Jul 3, 2014 |
| Received | Mar 14, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K140652
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.