FDA 510(k) Application Details - K071986

Device Classification Name	Mesh, Surgical   More FDA Info for this Device
510(K) Number	K071986
Device Name	Mesh, Surgical
Applicant	LIFECELL CORP. ONE MILLENNIUM WAY BRANCHBURG, NJ 08876 US Other 510(k) Applications for this Company
Contact	LORRAINE T MONTEMURRO Other 510(k) Applications for this Contact
Regulation Number	878.3300   More FDA Info for this Regulation Number
Classification Product Code	FTM Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/20/2007
Decision Date	10/19/2007
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review