510(k) K862311 ยท KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
SCREW DRIVER/BONE SCREW WRENCH/TAP & GUIDE PIN
| Applicant | Warsaw Orthopedic, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Jul 25, 1986 |
| Received | Jun 17, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862311
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.