510(k) K781389 ยท JDO Device, Fixation, Proximal Femoral, Implant
BIOMET CONCENTRIC HEX SCREW
| Applicant | Biomet, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 21, 1978 |
| Received | Aug 10, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K781389
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.