FDA 510(k) Application Details - K081327

Device Classification Name	Mesh, Surgical, Polymeric   More FDA Info for this Device
510(K) Number	K081327
Device Name	Mesh, Surgical, Polymeric
Applicant	HERNIAMESH S.R.L. 8 ORANGE DR. JERICHO, NY 11753 US Other 510(k) Applications for this Company
Contact	LORENA TRABUCCO 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	05/12/2008
Decision Date	06/19/2008
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