510(k) K073135 ยท LXT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite
SYNTHES (USA) HYBRID EXTERNAL FIXATOR MODIFICATIONS
| Applicant | Synthes (Usa), West Chester PA, US |
| Decision | Substantially Equivalent, Jan 29, 2008 |
| Received | Nov 7, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K073135
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.