510(k) K063158 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
SYNTHES ANTEGRA SYSTEM
| Applicant | Synthes Spine Co.Lp, West Chester PA, US |
| Decision | Substantially Equivalent, Nov 14, 2006 |
| Received | Oct 17, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K063158
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.