FDA 510(k) Applications Submitted by PAMELA VETTER

FDA 510(k) Number	Submission Date	Device Name	Applicant
K050161	01/25/2005	SYSTEM 7500-B ELECTROSURGICAL UNIT; ABCFLEX PROBE FOR FLEXIBLE ENDOSCOPY	CONMED ELECTROSURGERY
K170957	03/31/2017	ReConnex Pre-Sutured Tendon	AlloSource
K071849	07/05/2007	ALLOFUSE GEL AND PUTTY	ALLOSOURCE, INC.
K041868	07/09/2004	VALUPEN,PROFILE	CONMED CORPORATION
K052009	07/25/2005	CONMED SYSTEM MODEL 2450 ELECTROSURGICAL GENERATOR	CONMED CORPORATION
K052104	08/03/2005	ULTRACLEAN HANDCONTROLLED SUCTION COAGULATOR, MODEL 130182, 130183, 130184, 130185; ULTRACLEAN FOOTCONTROLLED SUCTION	CONMED CORPORATION
K103036	10/13/2010	ALLOFUSE PLUS	ALLOSOURCE, INC.