510(k) K093319 ยท KWP Appliance, Fixation, Spinal Interlaminal
NUVASIVE VUEPOINT OCT SYSTEM
| Applicant | Nuvasive, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Jun 23, 2010 |
| Received | Oct 23, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K093319
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.