510(k) K000742 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
SYNTHES ANTERIOR CSLP SYSTEM
| Applicant | Synthes Spine, Paoli PA, US |
| Decision | Substantially Equivalent, Mar 29, 2000 |
| Received | Mar 7, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K000742
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.