ClearanceBrief
510(k) K252240 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical

Spectrum Spine Cervical Cage System; Spectrum Spine Lumbar Cage System

ApplicantSpectrum Spine, Jasper GA, US
DecisionSubstantially Equivalent, Mar 30, 2026
ReceivedJul 17, 2025
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K252240

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.