ClearanceBrief
510(k) K261279 ยท OVE Intervertebral Fusion Device With Integrated Fixation, Cervical

DeltaNEC Interbody System

ApplicantNexus Spine, Salt Lake City UT, US
DecisionSubstantially Equivalent, Jun 22, 2026
ReceivedApr 17, 2026
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K261279

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.