510(k) K081568 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
ANTEGRA-T
| Applicant | Synthes Spine Co.Lp, West Chester PA, US |
| Decision | Substantially Equivalent, Sep 2, 2008 |
| Received | Jun 4, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K081568
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.