ClearanceBrief
510(k) K130306 ยท OVE Intervertebral Fusion Device With Integrated Fixation, Cervical

INCITE ANCHORED CERVICAL INTERBODY DEVICE

ApplicantIncite Innovation, LLC, Springfield MA, US
DecisionSubstantially Equivalent, Apr 11, 2013
ReceivedFeb 7, 2013
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K130306

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.