ClearanceBrief
510(k) K251617 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar

X-PAC® TLIF Expandable Posterior Cage System; X-PAC® LLIF Expandable Lateral Cage System

ApplicantExpanding Innovations, Inc., Mountain View CA, US
DecisionSubstantially Equivalent, Jun 16, 2025
ReceivedMay 27, 2025
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K251617

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.