510(k) K020274 ยท KXE Prosthesis, Wrist, Hemi-, Ulnar
WMT MODULAR ULNAR HEAD IMPLANT
| Applicant | Wrightmedicaltechnologyinc, Arlington TN, US |
| Decision | Substantially Equivalent, Feb 22, 2002 |
| Received | Jan 28, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020274
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.