ClearanceBrief
510(k) K180674 · ODP Intervertebral Fusion Device With Bone Graft, Cervical

EVOL® ha-C Cervical Interbody Fusion System

ApplicantCutting Edge Spine, LLC, Waxhaw NC, US
DecisionSubstantially Equivalent, Jun 25, 2018
ReceivedMar 15, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K180674

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.