510(k) K240424

Mineral Collagen Composite Bioactive Moldable Bone Graft Matrix by Collagen Matrix, Inc. — Product Code MQV

K240424 is an FDA 510(k) premarket notification submitted by Collagen Matrix, Inc. for the device "Mineral Collagen Composite Bioactive Moldable Bone Graft Matrix". The FDA issued a decision of Substantially Equivalent on March 12, 2024. The device falls under product code MQV (Filler, Bone Void, Calcium Compound), a Class II device regulated under 21 CFR 888.3045. Collagen Matrix, Inc. has at least 10 other 510(k) clearances on record.