510(k) K091692 ยท GXR Cover, Burr Hole
AESCULAP PEEK CRANIOFIX
| Applicant | Aesculap, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Aug 12, 2010 |
| Received | Jun 10, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K091692
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.