510(k) K030866 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
SYNTHES ANTERIOR CSLP SYSTEM
| Applicant | Synthes (Usa), West Chester PA, US |
| Decision | Substantially Equivalent, Apr 18, 2003 |
| Received | Mar 19, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K030866
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.