510(k) K970806 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
ACPII ANTERIOR CERVICAL PLATE SYSTEM
| Applicant | Sofamor Danek USA,Inc., Memphis TN, US |
| Decision | Substantially Equivalent for Some Indications, May 2, 1997 |
| Received | Mar 5, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970806
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.