510(k) K093808 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
INCITE INNOVATION STAND ALONE INTERBODY FUSION DEVICE
| Applicant | Incite Innovation, LLC, Springfield MA, US |
| Decision | Substantially Equivalent, Mar 24, 2010 |
| Received | Dec 11, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K093808
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.