ClearanceBrief
510(k) K251003 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar

X-PAC® LLIF Expandable Lateral Cage System

ApplicantExpanding Innovations, Inc., Mountain View CA, US
DecisionSubstantially Equivalent, Jun 25, 2025
ReceivedApr 1, 2025
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K251003

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.