510(k) K021342 ยท JEY Plate, Bone
NORMED BI-DIRECTIONAL/MULTIDIRECTIONAL JAW DISTRACTOR
| Applicant | Osteomedics, Inc., Paramus NJ, US |
| Decision | Substantially Equivalent, Aug 1, 2002 |
| Received | Apr 29, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K021342
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.