510(k) K932721 ยท HWC Screw, Fixation, Bone
ARTHROTEK SET SCREW
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent for Some Indications, Aug 1, 1994 |
| Received | Jun 4, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932721
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.