ClearanceBrief
510(k) K081917 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar

DEPUY SPINE BENGAL, CONCORDE, COUGAR, DEVEX AND LEOPARD SYSTEMS

ApplicantDepuy Spine, Inc., Raynham MA, US
DecisionSubstantially Equivalent, May 22, 2009
ReceivedJul 3, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K081917

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.