FDA 510(k) Application Details - K091921

Device Classification Name	Clip, Aneurysm   More FDA Info for this Device
510(K) Number	K091921
Device Name	Clip, Aneurysm
Applicant	Codman & Shurtleff, Inc. 325 PARAMOUNT DR. RAYNHAM, MA 02767-0350 US Other 510(k) Applications for this Company
Contact	PAUL AMARAL 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	06/30/2009
Decision Date	09/08/2009
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review