ClearanceBrief
510(k) K252219 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical

Cervical Interbody and VBR Fusion System

ApplicantSync Surgical, Plano TX, US
DecisionSubstantially Equivalent, Jan 14, 2026
ReceivedJul 15, 2025
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K252219

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.