FDA 510(k) Applications Submitted by MEDTRONIC AVE, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K011080 |
04/09/2001 |
BRIDGE SE SELF-EXPANDING STENT DELIVERY SYSTEM |
MEDTRONIC AVE, INC. |
| K011817 |
06/11/2001 |
BRIDGE FX |
MEDTRONIC AVE, INC. |
| K014205 |
12/21/2001 |
MODIFICATION TO BRIDGE SELF-EXPANDING BILIARY STENT DELIVERY SYSTEM (BRIDGE SE) |
MEDTRONIC AVE, INC. |
| K022026 |
06/21/2002 |
MEDTRONIC AVE BRIDGE POLARIS BILIARY STENT SYSTEM (POLARIS) |
MEDTRONIC AVE, INC. |
| K002346 |
08/02/2000 |
WIRE, GUIDE, CATHETER, MODEL QSW1000 |
MEDTRONIC AVE, INC. |
| K030839 |
03/17/2003 |
MEDTRONIC AVE BRIDGE AURORA BILIARY STENT SYSTEM (AURORA) |
MEDTRONIC AVE, INC. |
| K032768 |
09/08/2003 |
MEDTRONIC, INC. RACER BILIARY STENT SYSTEM (RACER), MODEL XD#YF(L) |
MEDTRONIC AVE, INC. |
| K030633 |
02/28/2003 |
MEDTRONIC AVE BRIDGE CONSTANT BILIARY STENT SYSTEM OR ('CONSTANT |
MEDTRONIC AVE, INC. |
| K994141 |
12/08/1999 |
CATHETER, INTRAVASCULAR OCCLUDING, TEMPORARY, MODEL SOL 3510; WIRE, GUIDE, CATHETER, MODEL QSW1000 |
MEDTRONIC AVE, INC. |
| K000744 |
03/07/2000 |
MEDTRONIC AVE BRIDGE X3 STENT |
MEDTRONIC AVE, INC. |
| K992318 |
07/12/1999 |
MEDTRONIC AVE BRIDGE STENT |
MEDTRONIC AVE, INC. |
| K992569 |
08/02/1999 |
MEDTRONIC AVE BRIDGE STENT |
MEDTRONIC AVE, INC. |
| K993145 |
09/20/1999 |
MEDTRONIC AVE BRIDGE STENT |
MEDTRONIC AVE, INC. |
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