510(k) K120854 ยท HRS Plate, Fixation, Bone
SYNTHES VA LCP ANKLE TRAUMA SYSTEM
| Applicant | Synthes USA, West Chester PA, US |
| Decision | Substantially Equivalent, Jun 18, 2012 |
| Received | Mar 21, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120854
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.