510(k) K982902

PERIPHERAL NERVE STIMULATION by Medtronic Vascular — Product Code GZF

K982902 is an FDA 510(k) premarket notification submitted by Medtronic Vascular for the device "PERIPHERAL NERVE STIMULATION". The FDA issued a decision of Substantially Equivalent on November 10, 1998. The device falls under product code GZF (Stimulator, Peripheral Nerve, Implanted (Pain Relief)), a Class II device regulated under 21 CFR 882.5870. Medtronic Vascular has at least 10 other 510(k) clearances on record.