510(k) K033930 ยท KXE Prosthesis, Wrist, Hemi-, Ulnar
KAPP CUSTOM ULNAR HEAD WRIST IMPLANT
| Applicant | Kapp Surgical Instrument, Inc., Warrensville OH, US |
| Decision | Substantially Equivalent, Jul 28, 2004 |
| Received | Dec 18, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K033930
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.