510(k) K053418 ยท KWP Appliance, Fixation, Spinal Interlaminal
SYNTHES OC FUSION SYSTEM
| Applicant | Synthes Spine Co.Lp, West Chester PA, US |
| Decision | Substantially Equivalent, Sep 6, 2006 |
| Received | Dec 8, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K053418
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.