510(k) K001793 ยท LXT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite
SYNTHES SCALLOPED DISTAL TIBIA PLATE
| Applicant | Synthes (Usa), Paoli PA, US |
| Decision | Substantially Equivalent, Aug 17, 2000 |
| Received | Jun 14, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001793
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.