510(k) K063017 ยท JDQ Cerclage, Fixation
AESCULAP STERNUMFIX STERNAL CLOSURE SYSTEM
| Applicant | Aesculap, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Dec 27, 2006 |
| Received | Oct 2, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K063017
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.