510(k) K982268 ยท KXE Prosthesis, Wrist, Hemi-, Ulnar
ULNAR HEAD IMPLANT
| Applicant | Avanta Orthopaedics, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Dec 4, 1998 |
| Received | Jun 29, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982268
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.