510(k) K031399

INTERGRO DBM by Interpore Cross Intl. — Product Code MQV

K031399 is an FDA 510(k) premarket notification submitted by Interpore Cross Intl. for the device "INTERGRO DBM". The FDA issued a decision of Substantially Equivalent on February 18, 2005. The device falls under product code MQV (Filler, Bone Void, Calcium Compound), a Class II device regulated under 21 CFR 888.3045. Interpore Cross Intl. has at least 10 other 510(k) clearances on record.