510(k) K071990 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
VALEO CERVICAL PLATE SYSTEM
| Applicant | Amedica Corp., Washington DC, US |
| Decision | Substantially Equivalent, Oct 29, 2007 |
| Received | Jul 20, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071990
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.