FDA 510(k) Application Details - K983831

Device Classification Name	Neurological Stereotaxic Instrument   More FDA Info for this Device
510(K) Number	K983831
Device Name	Neurological Stereotaxic Instrument
Applicant	BRAINLAB, AG 3100 HANSEN WAY PALO ALTO, CA 94304 US Other 510(k) Applications for this Company
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	10/30/1998
Decision Date	05/19/1999
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review