ClearanceBrief
510(k) K151198 ยท OVE Intervertebral Fusion Device With Integrated Fixation, Cervical

A-CIFT SoloFuse

ApplicantSpinefrontier, Inc., Beverly MA, US
DecisionSubstantially Equivalent, Jul 17, 2015
ReceivedMay 5, 2015
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K151198

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.