ClearanceBrief
510(k) K113465 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar

ACCULIF TL CAGE

ApplicantCoalign Innovations, Inc., Washington DC, US
DecisionSubstantially Equivalent, Dec 12, 2011
ReceivedNov 22, 2011
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K113465

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.