FDA 510(k) Application Details - K990469

Device Classification Name	Stimulator, Spinal-Cord, Implanted (Pain Relief)   More FDA Info for this Device
510(K) Number	K990469
Device Name	Stimulator, Spinal-Cord, Implanted (Pain Relief)
Applicant	ADVANCED NEUROMODULATION SYSTEMS ONE ALLENTOWN PKWY. ALLEN, TX 75002 US Other 510(k) Applications for this Company
Contact	DREW JOHNSON 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	02/16/1999
Decision Date	06/03/1999
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