FDA 510(k) Applications Submitted by GLEN D SMYTHE

FDA 510(k) Number	Submission Date	Device Name	Applicant
K020528	02/19/2002	INTRASTENT LD (LARGE DIAMETER) STENT	SULZER INTRATHERAPEUTICS, INC.
K050725	03/21/2005	PROTEGE GPS SELF-EXPANDING NITINOL STENT	EV3 CORPORATION
K051379	05/27/2005	PROTEGE RX GPS SELF-EXPANDING NITRINOL STENT	EV3 CORPORATION
K032206	07/18/2003	PARAMOUNT MINI STENT AND DELIVERY SYSTEM BILIARY INDICATION	EV3 INC
K042204	08/16/2004	MODIFICATION TO PROTEGE GPS SELF-EXPANDING NITINOL STENT	EV3 INC
K032580	08/21/2003	PROTEGE GPS SELF-EXPANDING NITINOL STENT AND DELIVERY SYSTEM	EV3 INC
K052659	09/27/2005	SPIDERX EMBOLIC PROTECTION DEVICE	EV3 INC
K033134	09/30/2003	MODIFICATION TO PARAMOUNT MINI STENT AND DELIVERY SYSTEM	EV3 INC
K033314	10/15/2003	PROTEGE GPS SELF-EXPANDING NITINOL STENT AND DELIVERY SYSTEM	EV3 INC
K043243	11/23/2004	PRIMUS STENT AND DELIVERY SYSTEM	EV3 INC