ClearanceBrief
510(k) K190067 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical

Velofix Interbody Fusion System

ApplicantU&I Corporation, Uijeongbu-Si, KR
DecisionSubstantially Equivalent, Feb 4, 2019
ReceivedJan 15, 2019
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K190067

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.