510(k) K242299

NovaBone Putty - Synthetic Bioactive Bone Graft by Novabone Products, LLC — Product Code MQV

K242299 is an FDA 510(k) premarket notification submitted by Novabone Products, LLC for the device "NovaBone Putty - Synthetic Bioactive Bone Graft". The FDA issued a decision of Substantially Equivalent on September 25, 2024. The device falls under product code MQV (Filler, Bone Void, Calcium Compound), a Class II device regulated under 21 CFR 888.3045. Novabone Products, LLC has at least 10 other 510(k) clearances on record.