FDA 510(k) Application Details - K010300

Device Classification Name	Stimulator, Spinal-Cord, Implanted (Pain Relief)   More FDA Info for this Device
510(K) Number	K010300
Device Name	Stimulator, Spinal-Cord, Implanted (Pain Relief)
Applicant	MEDTRONIC VASCULAR 800 53RD AVENUE, N.E. MINNEAPOLIS, MN 55421 US Other 510(k) Applications for this Company
Contact	PAM SCHAUB Other 510(k) Applications for this Contact
Regulation Number	882.5880   More FDA Info for this Regulation Number
Classification Product Code	GZB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/01/2001
Decision Date	08/01/2001
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review