510(k) K001614 ยท KTW Appliance, Fixation, Nail/Blade/Plate Combination, Single Component
STRYKER TRAUMA PELVIC SET
| Applicant | Howmedica Osteonics Corp., Allendale NJ, US |
| Decision | Substantially Equivalent, Aug 4, 2000 |
| Received | May 25, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001614
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.