510(k) K082874 ยท HWC Screw, Fixation, Bone
BIODRIVE CANNULATED SCREW SYSTEM
| Applicant | Biomet Trauma, Parsippany NJ, US |
| Decision | Substantially Equivalent, Feb 5, 2009 |
| Received | Sep 29, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082874
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.