Company ยท US
The Heart Valve Div. Medtronic Cardiovascular Surg
FDA 510(k) clearances and medical device recalls filed under this name, 1991 to 1998. Name variants (Inc, Corp, punctuation) are merged.
5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Apr 30, 1998 | K980534 | DURAN FLEXIBLE ANNULOPLASTY RING MODEL NUMBER H608H The Heart Valve Div. Medtronic Cardiovascular Surg | KRH |
| Aug 27, 1996 | K960356 | POSTERIOR ANNULOPLASTY BAND (MODEL 607) The Heart Valve Div. Medtronic Cardiovascular Surg | KRH |
| Jul 14, 1995 | K944956 | UNIPOLAR PEDIATRIC TEMPORARY PACING LEAD, MODEL 6491 The Heart Valve Div. Medtronic Cardiovascular Surg | LDF |
| Nov 23, 1992 | K922269 | UNIPOLAR TEMPORARY MYOCARDIAL PACING WIRE, 6493 The Heart Valve Div. Medtronic Cardiovascular Surg | LDF |
| Nov 22, 1991 | K914602 | DURAN FLEX ANNULOPLASTY RING/OBTUR H601H, MODIFIED The Heart Valve Div. Medtronic Cardiovascular Surg | KRH |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||