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Sulzer Intratherapeutics, Inc.

8 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
MODIFICATION TO PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY (K023243)Sulzer Intratherapeutics, Inc.2002-12-13
MODIFICATION TO PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY (K021729)Sulzer Intratherapeutics, Inc.2002-06-21
INTRACOIL SELF-EXPANDING PERIPHERAL STENT (K021563)Sulzer Intratherapeutics, Inc.2002-05-31
INTRASTENT LD (LARGE DIAMETER) STENT (K020528)Sulzer Intratherapeutics, Inc.2002-04-16
MODIFICATION TO PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY (K014136)Sulzer Intratherapeutics, Inc.2002-01-17
PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY (K011806)Sulzer Intratherapeutics, Inc.2001-09-07
PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY (K012347)Sulzer Intratherapeutics, Inc.2001-08-23
PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY (K012066)Sulzer Intratherapeutics, Inc.2001-08-01

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Every clearance here is in the API, with alerts when new ones post.