510(k) K063205

ATLAS SPINE VERTEBRAL BODY REPLACEMENT by Atlas Spine, LLC — Product Code MQP

K063205 is an FDA 510(k) premarket notification submitted by Atlas Spine, LLC for the device "ATLAS SPINE VERTEBRAL BODY REPLACEMENT". The FDA issued a decision of Substantially Equivalent on February 26, 2007. The device falls under product code MQP (Spinal Vertebral Body Replacement Device), a Class II device regulated under 21 CFR 888.3060. Atlas Spine, LLC has at least 10 other 510(k) clearances on record.