510(k) K926453 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
SYNTHES (U.S.A.) ANTERIOR CERVICAL VERTEBRAE PLATE
| Applicant | Synthes (Usa), Paoli PA, US |
| Decision | Substantially Equivalent for Some Indications, Oct 12, 1993 |
| Received | Dec 24, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K926453
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.