510(k) K032634 ยท JDS Nail, Fixation, Bone
NORMED COMPRESSION BONE SCREW SYSTEM
| Applicant | Noviace Corporation, Paramus NJ, US |
| Decision | Substantially Equivalent, Oct 6, 2003 |
| Received | Aug 26, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K032634
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.