510(k) K130868

NUVASIVE DECADE LATERAL PLATE SYSTEM by Nuvasive, Inc. — Product Code KWQ

K130868 is an FDA 510(k) premarket notification submitted by Nuvasive, Inc. for the device "NUVASIVE DECADE LATERAL PLATE SYSTEM". The FDA issued a decision of Substantially Equivalent on August 29, 2013. The device falls under product code KWQ (Appliance, Fixation, Spinal Intervertebral Body), a Class II device regulated under 21 CFR 888.3060. Nuvasive, Inc. has at least 10 other 510(k) clearances on record.