510(k) K050028 ยท KWN Prosthesis, Wrist, Carpal Lunate
MAESTRO CARPAL HEMIARTHROPLASTY
| Applicant | Biomet Manufacturing, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Mar 25, 2005 |
| Received | Jan 6, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K050028
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.