FDA 510(k) Application Details - K022222

Device Classification Name	Stimulator, Spinal-Cord, Implanted (Pain Relief)   More FDA Info for this Device
510(K) Number	K022222
Device Name	Stimulator, Spinal-Cord, Implanted (Pain Relief)
Applicant	ADVANCED NEUROMODULATION SYSTEM,INC 6501 WINDCREST DRIVE,SUTE 100 PLANO, TX 75024 US Other 510(k) Applications for this Company
Contact	KATRYNA WARREN 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	07/09/2002
Decision Date	08/08/2002
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