510(k) K130868 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
NUVASIVE DECADE LATERAL PLATE SYSTEM
| Applicant | Nuvasive, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Aug 29, 2013 |
| Received | Mar 29, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130868
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.