510(k) K010321 ยท KTW Appliance, Fixation, Nail/Blade/Plate Combination, Single Component
MODULAR FOOT SYSTEM - 2.7 MM MODULE
| Applicant | Synthes (Usa), Paoli PA, US |
| Decision | Substantially Equivalent, May 2, 2001 |
| Received | Feb 2, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K010321
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.