Medtronic Ave, Inc. - FDA 510(k) Cleared Devices
13
Total
2
Cleared
0
Denied
Medtronic Ave, Inc. has 2 FDA 510(k) cleared gastroenterology & urology devices. Based in Santa Rosa, US.
Historical record: 2 cleared submissions from 1999 to 2003.
Browse the complete list of FDA 510(k) cleared gastroenterology & urology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Medtronic Ave, Inc.
13 devices
Cleared
Oct 09, 2003
MEDTRONIC, INC. RACER BILIARY STENT SYSTEM (RACER), MODEL XD#YF(L)
Gastroenterology & Urology
31d
Cleared
Sep 02, 2003
MEDTRONIC AVE BRIDGE CONSTANT BILIARY STENT SYSTEM OR ('CONSTANT
Gastroenterology & Urology
186d
Cleared
May 30, 2003
MEDTRONIC AVE BRIDGE AURORA BILIARY STENT SYSTEM (AURORA)
Gastroenterology & Urology
74d
Cleared
Jul 19, 2002
MEDTRONIC AVE BRIDGE POLARIS BILIARY STENT SYSTEM (POLARIS)
Gastroenterology & Urology
28d
Cleared
Jan 14, 2002
MODIFICATION TO BRIDGE SELF-EXPANDING BILIARY STENT DELIVERY SYSTEM (BRIDGE SE)
Gastroenterology & Urology
24d
Cleared
Oct 11, 2001
BRIDGE SE SELF-EXPANDING STENT DELIVERY SYSTEM
Gastroenterology & Urology
185d
Cleared
Aug 22, 2001
BRIDGE FX
Gastroenterology & Urology
72d
Cleared
Sep 27, 2000
WIRE, GUIDE, CATHETER, MODEL QSW1000
Cardiovascular
56d
Cleared
Jul 21, 2000
CATHETER, INTRAVASCULAR OCCLUDING, TEMPORARY, MODEL SOL 3510
Cardiovascular
226d
Cleared
Jun 05, 2000
MEDTRONIC AVE BRIDGE X3 STENT
Gastroenterology & Urology
90d
Cleared
Oct 21, 1999
MEDTRONIC AVE BRIDGE STENT
Gastroenterology & Urology
31d
Cleared
Aug 31, 1999
MEDTRONIC AVE BRIDGE STENT
Gastroenterology & Urology
29d