FDA 510(k) Application Details - K003519

Device Classification Name	Clip, Aneurysm   More FDA Info for this Device
510(K) Number	K003519
Device Name	Clip, Aneurysm
Applicant	AESCULAP, INC. 944 MARCON BLVD. ALLENTOWN, PA 18109 US Other 510(k) Applications for this Company
Contact	JOYCE THOMAS 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	11/15/2000
Decision Date	01/29/2001
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