510(k) K010964 ยท HWC Screw, Fixation, Bone
AUTO-DRIVE LAG SCREW SYSTEM
| Applicant | Osteomed Corp., Addison TX, US |
| Decision | Substantially Equivalent, Jul 5, 2001 |
| Received | Mar 30, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K010964
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.