510(k) K081243 ยท HSB Rod, Fixation, Intramedullary And Accessories
BIOMET PHOENIX ANKLE NAIL SYSTEM
| Applicant | Biomet Trauma, Warsaw IN, US |
| Decision | Substantially Equivalent, Jun 27, 2008 |
| Received | May 1, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K081243
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.