510(k) K070148 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
GRAFT CONTAINMENT DEVICE
| Applicant | Nuvasive, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Jul 31, 2007 |
| Received | Jan 16, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070148
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.