510(k) K080992 ยท HRS Plate, Fixation, Bone
AESCULAP IMPLANT SYSTEMS HIGH TIBIAL OSTEOTOMY PLATING SYSTEM
| Applicant | Aesculap Implant Systems, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Sep 4, 2008 |
| Received | Apr 7, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K080992
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.