510(k) K100043 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
COROENT XLR STANDALONE SYSTEM
| Applicant | Nuvasive, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Jun 16, 2010 |
| Received | Jan 8, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K100043
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.