510(k) K790125 ยท KXE Prosthesis, Wrist, Hemi-, Ulnar
ULNAR HEAD PROTHESIS
| Applicant | Cutter Laboratories, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 8, 1979 |
| Received | Jan 23, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K790125
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.