FDA 510(k) Application Details - K072462

Device Classification Name	Stimulator, Spinal-Cord, Implanted (Pain Relief)   More FDA Info for this Device
510(K) Number	K072462
Device Name	Stimulator, Spinal-Cord, Implanted (Pain Relief)
Applicant	ADVANCED NEUROMODULATION SYSTEMS 6901 PRESTON RD. PLANO, TX 75024 US Other 510(k) Applications for this Company
Contact	MIA M WARE 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	08/31/2007
Decision Date	10/11/2007
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Statement
Type	Special
Reviewed By Third Party	N
Expedited Review