510(k) K880214 ยท KWP Appliance, Fixation, Spinal Interlaminal
TSRH H/M TORQUE LIMITING WRENCH
| Applicant | Warsaw Orthopedic, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Feb 18, 1988 |
| Received | Jan 19, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880214
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.