510(k) K021618 ยท JEY Plate, Bone
OSA RIGID INTERNAL FIXATION SYSTEM
| Applicant | Osteomed Corp., Addison TX, US |
| Decision | Substantially Equivalent, Aug 8, 2002 |
| Received | May 16, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K021618
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.