The Heart Valve Div. Medtronic Cardiovascular Surg
FDA 510(k) & PMA Approved Devices — 5 products
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Total Devices5
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K980534 | DURAN FLEXIBLE ANNULOPLASTY RING MODEL NUMBER H608H | KRH | 1998-04-30 | View |
| 510(k) | K960356 | POSTERIOR ANNULOPLASTY BAND (MODEL 607) | KRH | 1996-08-27 | View |
| 510(k) | K944956 | UNIPOLAR PEDIATRIC TEMPORARY PACING LEAD, MODEL 6491 | LDF | 1995-07-14 | View |
| 510(k) | K922269 | UNIPOLAR TEMPORARY MYOCARDIAL PACING WIRE, 6493 | LDF | 1992-11-23 | View |
| 510(k) | K914602 | DURAN FLEX ANNULOPLASTY RING/OBTUR H601H, MODIFIED | KRH | 1991-11-22 | View |
No matching devices.
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