510(k) K131723 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
COROENT SINGLE TAB SYSTEM
| Applicant | Nuvasive, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Sep 20, 2013 |
| Received | Jun 12, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131723
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.