ClearanceBrief
510(k) K110454 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar

COUGAR LS LATERAL CAGE SYSTEM

ApplicantJohnson & Johnson, Raynham MA, US
DecisionSubstantially Equivalent, May 13, 2011
ReceivedFeb 16, 2011
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K110454

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.