FDA 510(k) Application Details - K061208

Device Classification Name	Dura Substitute   More FDA Info for this Device
510(K) Number	K061208
Device Name	Dura Substitute
Applicant	LIFECELL CORP. ONE MILLENIUM WAY BRANCHBURG, NJ 08876 US Other 510(k) Applications for this Company
Contact	REY LIBROJO Other 510(k) Applications for this Contact
Regulation Number	882.5910   More FDA Info for this Regulation Number
Classification Product Code	GXQ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/01/2006
Decision Date	01/03/2007
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