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Sulzer Intratherapeutics, Inc.

FDA 510(k) & PMA Approved Devices — 8 products

Total Devices8

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K023243	MODIFICATION TO PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY	FGE	2002-12-13	View
510(k)	K021729	MODIFICATION TO PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY	FGE	2002-06-21	View
510(k)	K021563	INTRACOIL SELF-EXPANDING PERIPHERAL STENT	JCT	2002-05-31	View
510(k)	K020528	INTRASTENT LD (LARGE DIAMETER) STENT	FGE	2002-04-16	View
510(k)	K014136	MODIFICATION TO PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY	FGE	2002-01-17	View
510(k)	K011806	PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY	FGE	2001-09-07	View
510(k)	K012347	PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY	FGE	2001-08-23	View
510(k)	K012066	PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY	FGE	2001-08-01	View

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