510(k) K973309 ยท HWC Screw, Fixation, Bone
VILEX CANNULATED BONE SCREW, DUVAL CANNULATED BONE SCREW
| Applicant | Vilex, Inc., Large PA, US |
| Decision | Substantially Equivalent for Some Indications, Jan 16, 1998 |
| Received | Sep 3, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973309
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.