FDA 510(k) Application Details - K971617

Device Classification Name	Shunt, Central Nervous System And Components   More FDA Info for this Device
510(K) Number	K971617
Device Name	Shunt, Central Nervous System And Components
Applicant	INTEGRA NEUROCARE LLC. 8401 102ND ST. SUITE 200-P.O. BOX 390 PLEASANT PRAIRIE, WI 53150-0390 US Other 510(k) Applications for this Company
Contact	LORI L HAYS Other 510(k) Applications for this Contact
Regulation Number	882.5550   More FDA Info for this Regulation Number
Classification Product Code	JXG Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/02/1997
Decision Date	07/31/1997
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