510(k) K113121 ยท PHX Shoulder Prosthesis, Reverse Configuration
COMPREHENSIVE REVERSE SHOULDER
| Applicant | Biomet Manufacturing, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Dec 16, 2011 |
| Received | Oct 21, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K113121
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.