510(k) K072339 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
NUVASIVE ANTERIOR LUMBAR PLATE SYSTEM
| Applicant | Nuvasive, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Oct 19, 2007 |
| Received | Aug 20, 2007 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K072339
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.