510(k) K843554 ยท KTW Appliance, Fixation, Nail/Blade/Plate Combination, Single Component
BONE SCREWS
| Applicant | Mecron Medical Products, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Oct 1, 1984 |
| Received | Sep 10, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K843554
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.