510(k) K062590 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
NUVASIVE ACP4 SYSTEM
| Applicant | Nuvasive, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Jan 18, 2007 |
| Received | Sep 1, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K062590
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.