510(k) K111866 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
NUVASIVE ANTERIOR LUMBAR PLATE SYSTEM
| Applicant | Nuvasive, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Jul 22, 2011 |
| Received | Jun 30, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K111866
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.