510(k) K891066 ยท KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
DANEK WRIST FIXATOR
| Applicant | Danek Medical, Inc., Memphis TN, US |
| Decision | Substantially Equivalent, Aug 28, 1989 |
| Received | Mar 1, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K891066
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.