Sulzer Intratherapeutics, Inc. - FDA 510(k) Cleared Devices
8
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Sulzer Intratherapeutics, Inc. Gastroenterology & Urology ✕
7 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
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