FDA 510(k) Application Details - K083597

Device Classification Name	Neurological Stereotaxic Instrument   More FDA Info for this Device
510(K) Number	K083597
Device Name	Neurological Stereotaxic Instrument
Applicant	SONOWAND AS 435 RICE CREEK TERRACE FRIDLEY, MN 55432 US Other 510(k) Applications for this Company
Contact	CONSTANCE G BUNDY Other 510(k) Applications for this Contact
Regulation Number	882.4560   More FDA Info for this Regulation Number
Classification Product Code	HAW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/05/2008
Decision Date	09/25/2009
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