510(k) K896404 ยท JEY Plate, Bone
TITAMED ANTWERP SYSTEM
| Applicant | Optik, Criftib MD, US |
| Decision | Substantially Equivalent, Apr 16, 1990 |
| Received | Nov 7, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896404
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.