510(k) K950384 ยท LXT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite
SYNTHES(USA) SYNTHES HYBRID EXTERNAL FIXATOR
| Applicant | Synthes (Usa), Paoli PA, US |
| Decision | Substantially Equivalent, May 22, 1995 |
| Received | Feb 1, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K950384
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.