ClearanceBrief
510(k) K180364 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical

HD LifeSciences Cervical IBFD System

ApplicantHd Lifesciences, LLC, Stoneham MA, US
DecisionSubstantially Equivalent, Jun 27, 2018
ReceivedFeb 12, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K180364

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.