FDA 510(k) Application Details - K063556

Device Classification Name	Mesh, Surgical   More FDA Info for this Device
510(K) Number	K063556
Device Name	Mesh, Surgical
Applicant	PM DEVICES, INC. 13700 MAYFIELD PL. UNIT 2135 RICHMOND V6V 2E4 CA Other 510(k) Applications for this Company
Contact	TIM VERSPAGEN 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	11/27/2006
Decision Date	03/20/2007
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review