510(k) K001922 ยท KYJ Prosthesis, Finger, Constrained, Polymer
DEPUY NEUFLEX PIP FINGER
| Applicant | Depuy, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Aug 29, 2000 |
| Received | Jun 23, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001922
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.