ClearanceBrief
510(k) K092574 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar

ESL SPINAL SYSTEM

ApplicantEbi, L.P., Parsippany NJ, US
DecisionSubstantially Equivalent, Feb 4, 2010
ReceivedAug 21, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K092574

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.