510(k) K931686 ยท KTW Appliance, Fixation, Nail/Blade/Plate Combination, Single Component
MALLEOLAR SCREW
| Applicant | Onyx Medical Corp., Memphis TN, US |
| Decision | Substantially Equivalent, Apr 5, 1994 |
| Received | Apr 5, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K931686
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.