FDA 510(k) Applications Submitted by DIANA M BORDON

FDA 510(k) Number	Submission Date	Device Name	Applicant
K021792	05/31/2002	BILAYER MATRIX WOUND DRESSING	INTEGRA LIFESCIENCES CORP.
K081635	06/11/2008	INTEGRA MESHED BILAYER WOUND MATRIX	INTEGRA LIFESCIENCES CORP.
K041620	06/16/2004	NEURA WRAP NERVE PROTECTOR	INTEGRA LIFESCIENCES CORP.
K072113	08/01/2007	INTEGRA FLOWABLE WOUND MATRIX, MODEL FWD301	INTEGRA LIFESCIENCES CORP.
K062353	08/11/2006	MOZAIK BONE REGENERATION MATRIX - PUTTY	INTEGRA LIFESCIENCES CORPORATION
K032693	09/02/2003	DURAGEN PLUS DURAL GRAFT MATRIX	INTEGRA LIFESCIENCES CORP.
K063124	10/13/2006	INTEGRA MOZAIK BONE REGENERATION MATRIX - STRIPS	INTEGRA LIFESCIENCES CORP.
K043427	12/13/2004	DURAGEN II DURAL REGENERATION MATRIX	INTEGRA LIFESCIENCES CORP.
K053655	12/30/2005	TENDON WRAP TENDON PROTECTOR	INTEGRA LIFESCIENCES CORPORATION