FDA 510(k) Application Details - K013625

Device Classification Name	Mesh, Surgical   More FDA Info for this Device
510(K) Number	K013625
Device Name	Mesh, Surgical
Applicant	TISSUE SCIENCE LABORATORIES, PLC 555 THIRTEENTH ST. N.W. WASHINGTON, DC 20004-1109 US Other 510(k) Applications for this Company
Contact	HOWARD M HOLSTEIN 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	11/05/2001
Decision Date	01/17/2002
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