FDA 510(k) Application Details - K990202

Device Classification Name	Clip, Aneurysm   More FDA Info for this Device
510(K) Number	K990202
Device Name	Clip, Aneurysm
Applicant	MIZUHO AMERICA, INC. 12300 TWINBROOK PKWY. SUITE 625 ROCKVILLE, MD 20852 US Other 510(k) Applications for this Company
Contact	T.WHIT ATHEY Other 510(k) Applications for this Contact
Regulation Number	882.5200   More FDA Info for this Regulation Number
Classification Product Code	HCH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/21/1999
Decision Date	06/04/1999
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