510(k) K070891 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
ALTIVA CLASSIC ACP SYSTEM
| Applicant | Altiva Corp., Charlotte NC, US |
| Decision | Substantially Equivalent, Jun 11, 2007 |
| Received | Mar 30, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070891
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.