510(k) K122008 ยท OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
INCITE ANCHORED CERVICAL INTERBODY (ACI) FUSION DEVICE
| Applicant | Incite Innovation, LLC, Springfield MA, US |
| Decision | Substantially Equivalent, Nov 16, 2012 |
| Received | Jul 9, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122008
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.