510(k) K082070 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
NUVASIVE LATERAL PLATE SYSTEM
| Applicant | Nuvasive, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Sep 24, 2008 |
| Received | Jul 22, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K082070
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.