FDA 510(k) Application Details - K100787

Device Classification Name	Mesh, Surgical, Polymeric   More FDA Info for this Device
510(K) Number	K100787
Device Name	Mesh, Surgical, Polymeric
Applicant	SMITH & NEPHEW, INC. 970 LAKE CARILLON DR. SUITE 110 ST. PETERSBURG, FL 33716 US Other 510(k) Applications for this Company
Contact	LAURA D REYNOLDS Other 510(k) Applications for this Contact
Regulation Number	878.3300   More FDA Info for this Regulation Number
Classification Product Code	FTL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/19/2010
Decision Date	09/17/2010
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