FDA 510(k) Application Details - K073391

Device Classification Name	Mesh, Surgical   More FDA Info for this Device
510(K) Number	K073391
Device Name	Mesh, Surgical
Applicant	COOK BIOTECH, INC. 1425 INNOVATION PLACE WEST LAFAYETTE, IN 47906-1000 US Other 510(k) Applications for this Company
Contact	MARY A FADERAN 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	12/03/2007
Decision Date	03/21/2008
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