510(k) K042902 ยท KXE Prosthesis, Wrist, Hemi-, Ulnar
HERBERT ULNAR HEAD PROSTHESIS SYSTEM
| Applicant | Stuckenbrock Medizintechnik GmbH, Miami FL, US |
| Decision | Substantially Equivalent, Dec 27, 2004 |
| Received | Oct 20, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K042902
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.