510(k) K053581 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
NUVASIVE SMARTPLATE GRADIENT PLUS SYSTEM
| Applicant | Nuvasive, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Feb 17, 2006 |
| Received | Dec 23, 2005 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K053581
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.