510(k) K091218

DBX DEMINERALIZED BONE MATRIX PUTTY by Musculoskeletal Transplant Foundation — Product Code MQV

K091218 is an FDA 510(k) premarket notification submitted by Musculoskeletal Transplant Foundation for the device "DBX DEMINERALIZED BONE MATRIX PUTTY". The FDA issued a decision of Substantially Equivalent on September 28, 2009. The device falls under product code MQV (Filler, Bone Void, Calcium Compound), a Class II device regulated under 21 CFR 888.3045. Musculoskeletal Transplant Foundation has at least 10 other 510(k) clearances on record.