FDA 510(k) Applications Submitted by EDWARD F KENT

FDA 510(k) Number	Submission Date	Device Name	Applicant
K970119	01/14/1997	MITEK ABSORBABLE POLYDIOXANONE (PDS) H FIX	MITEK PRODUCTS
K970360	01/31/1997	MITEK SUTURE RETROGRADER	MITEK PRODUCTS
K961094	03/14/1996	MITEK THREADED ANCHOR (MODIFICATION)	MITEK PRODUCTS
K982420	06/15/1998	MITEK MICRO ANCHOR	MITEK PRODUCTS
K962511	06/27/1996	MITEK MICRO ANCHOR	MITEK PRODUCTS
K962793	07/17/1996	MITEK MICRO ANCHOR	MITEK PRODUCTS
K953560	07/20/1995	MITEK THREADED ANCHOR (FASTIN)	MITEK SURGICAL PRODUCTS, INC.
K973009	08/13/1997	MITEK NON ABSORBABLE POLYPROPYLENE H FIX	MITEK PRODUCTS
K963783	09/20/1996	MITEK ELECTROSURGICAL SYSTEM FOR ARTHROSCOPIC USE	ETHICON, INC.
K964013	10/07/1996	MITEK ABSORBABLE TOGGLE ANCHOR	MITEK PRODUCTS
K974022	10/14/1997	VAPR	MITEK PRODUCTS
K983818	10/29/1998	MITEK FASTIN RC ANCHOR	MITEK PRODUCTS
K974291	11/14/1997	MITEK BTB ABSORBABLE (PLA) CROSS PIN	MITEK PRODUCTS
K974345	11/19/1997	MITEK KNOTLESS ANCHOR	MITEK PRODUCTS