510(k) K060492 ยท JEY Plate, Bone
AESCULAP CRANIOFACIAL PLATE AND SCREW
| Applicant | Aesculap, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Apr 7, 2006 |
| Received | Feb 24, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K060492
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.