510(k) K241802

Device 300397 Putty by Geistlich Pharma AG — Product Code MQV

K241802 is an FDA 510(k) premarket notification submitted by Geistlich Pharma AG for the device "Device 300397 Putty". The FDA issued a decision of Substantially Equivalent on November 8, 2024. The device falls under product code MQV (Filler, Bone Void, Calcium Compound), a Class II device regulated under 21 CFR 888.3045. Geistlich Pharma AG has at least 10 other 510(k) clearances on record.