Medtronic Ave, Inc.
FDA 510(k) & PMA Approved Devices — 13 products
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Total Devices13
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K032768 | MEDTRONIC, INC. RACER BILIARY STENT SYSTEM (RACER), MODEL XD#YF(L) | FGE | 2003-10-09 | View |
| 510(k) | K030633 | MEDTRONIC AVE BRIDGE CONSTANT BILIARY STENT SYSTEM OR ('CONSTANT | FGE | 2003-09-02 | View |
| 510(k) | K030839 | MEDTRONIC AVE BRIDGE AURORA BILIARY STENT SYSTEM (AURORA) | FGE | 2003-05-30 | View |
| 510(k) | K022026 | MEDTRONIC AVE BRIDGE POLARIS BILIARY STENT SYSTEM (POLARIS) | FGE | 2002-07-19 | View |
| 510(k) | K014205 | MODIFICATION TO BRIDGE SELF-EXPANDING BILIARY STENT DELIVERY SYSTEM (BRIDGE SE) | FGE | 2002-01-14 | View |
| 510(k) | K011080 | BRIDGE SE SELF-EXPANDING STENT DELIVERY SYSTEM | FGE | 2001-10-11 | View |
| 510(k) | K011817 | BRIDGE FX | FGE | 2001-08-22 | View |
| 510(k) | K002346 | WIRE, GUIDE, CATHETER, MODEL QSW1000 | DQX | 2000-09-27 | View |
| 510(k) | K994141 | CATHETER, INTRAVASCULAR OCCLUDING, TEMPORARY, MODEL SOL 3510; WIRE, GUIDE, CATHETER, MODEL QSW1000 | MJN | 2000-07-21 | View |
| 510(k) | K000744 | MEDTRONIC AVE BRIDGE X3 STENT | FGE | 2000-06-05 | View |
| 510(k) | K993145 | MEDTRONIC AVE BRIDGE STENT | FGE | 1999-10-21 | View |
| 510(k) | K992569 | MEDTRONIC AVE BRIDGE STENT | FGE | 1999-08-31 | View |
| 510(k) | K992318 | MEDTRONIC AVE BRIDGE STENT | FGE | 1999-08-02 | View |
No matching devices.
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