510(k) K092812 ยท HRS Plate, Fixation, Bone
SYNTHES (USA) 2.7MM/ 3.5MM LCP ANTEROLATERAL DISTAL TIBIA PLATES
| Applicant | Synthes (Usa), West Chester PA, US |
| Decision | Substantially Equivalent, May 11, 2010 |
| Received | Sep 14, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092812
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.