510(k) K082037 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
SEEPLATE CERVICAL PLATE SYSTEM
| Applicant | Amedica Corp., Washington DC, US |
| Decision | Substantially Equivalent, Sep 26, 2008 |
| Received | Jul 17, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K082037
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.