510(k) K973231 ยท KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
THE CORIFIX DYNAMIC HIP SCREW SYSTEM
| Applicant | Corin USA, Tampa FL, US |
| Decision | Substantially Equivalent, Nov 20, 1997 |
| Received | Aug 27, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973231
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.