510(k) K121183 ยท PHX Shoulder Prosthesis, Reverse Configuration
COMPREHENSIVE REVERSE SHOULDER - E1 POLYETHYLENE CLAIMS
| Applicant | Biomet Corporation, Warsaw IN, US |
| Decision | Substantially Equivalent, Jul 26, 2012 |
| Received | Apr 18, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K121183
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.