510(k) K023022 ยท HWC Screw, Fixation, Bone
NUGEN FX SCREW
| Applicant | Bionx Implants, Inc., Blue Bell PA, US |
| Decision | Substantially Equivalent, Oct 4, 2002 |
| Received | Sep 11, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K023022
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.