510(k) K781762 ยท KTW Appliance, Fixation, Nail/Blade/Plate Combination, Single Component
COMPRESSION HIP SCREW SYSTEM
| Applicant | Howmedica Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 20, 1978 |
| Received | Oct 16, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K781762
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.