510(k) K012798 ยท HWC Screw, Fixation, Bone
INTEX SCREW
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Nov 16, 2001 |
| Received | Aug 21, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K012798
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.