510(k) K032520 ยท JEY Plate, Bone
ORTRAUTEK TRAUMA SYSTEM
| Applicant | Tekka, Bethesda MD, US |
| Decision | Substantially Equivalent, Nov 12, 2003 |
| Received | Aug 15, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K032520
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.