510(k) K781668 ยท KYJ Prosthesis, Finger, Constrained, Polymer
GAMMA RADIATION STERILIZATION PRECEDURE
| Applicant | Cutter Laboratories, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Nov 3, 1978 |
| Received | Sep 28, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K781668
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.