ClearanceBrief
510(k) K221162 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical

UniVy OsteoVy Cervical IBF System

ApplicantVy Spine, LLC, Tallahassee FL, US
DecisionSubstantially Equivalent, Nov 4, 2022
ReceivedApr 22, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K221162

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.