FDA 510(k) Application Details - K101851

Device Classification Name	Mesh, Surgical, Polymeric   More FDA Info for this Device
510(K) Number	K101851
Device Name	Mesh, Surgical, Polymeric
Applicant	DAVOL INC., SUB. C.R. BARD, INC. 100 CROSSINGS BLVD WARWICK, RI 02886 US Other 510(k) Applications for this Company
Contact	MICHELLE GODIN 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	07/01/2010
Decision Date	07/15/2010
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Statement
Type	Special
Reviewed By Third Party	N
Expedited Review