510(k) K070922 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
MODIFICATION TO SPINAL USA VBR SYSTEM
| Applicant | Spinal USA, Flowood MS, US |
| Decision | Substantially Equivalent, Sep 19, 2007 |
| Received | Apr 2, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070922
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.