510(k) K103750 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
NUVASIVE TRAVERSE PLATE SYSTEM
| Applicant | Nuvasive, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Mar 3, 2011 |
| Received | Dec 23, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K103750
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.