Sulzer Intratherapeutics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sulzer Intratherapeutics, Inc. - FDA 510(k) Cleared Devices
8
Total
2
Cleared
0
Denied
Sulzer Intratherapeutics, Inc. has 2 FDA 510(k) cleared medical devices. Based in Saint Paul, US.
Historical record: 2 cleared submissions from 2001 to 2002. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Sulzer Intratherapeutics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sulzer Intratherapeutics, Inc.
8 devices
Cleared
Dec 13, 2002
MODIFICATION TO PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY...
Gastroenterology & Urology
74d
Cleared
Jun 21, 2002
MODIFICATION TO PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY...
Gastroenterology & Urology
28d
Cleared
May 31, 2002
INTRACOIL SELF-EXPANDING PERIPHERAL STENT
General & Plastic Surgery
18d
Cleared
Apr 16, 2002
INTRASTENT LD (LARGE DIAMETER) STENT
Gastroenterology & Urology
56d
Cleared
Jan 17, 2002
MODIFICATION TO PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY...
Gastroenterology & Urology
31d
Cleared
Sep 07, 2001
PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY
Gastroenterology & Urology
88d
Cleared
Aug 23, 2001
PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY
Gastroenterology & Urology
30d
Cleared
Aug 01, 2001
PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY
Gastroenterology & Urology
30d