ClearanceBrief
510(k) K110270 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar

ACCULIF CAGE

ApplicantCoalign Innovations, Inc., Washington DC, US
DecisionSubstantially Equivalent, Apr 7, 2011
ReceivedJan 31, 2011
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K110270

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.