The Heart Valve Div. Medtronic Cardiovascular Surg - FDA 510(k) Clear...
5
Total
4
Cleared
0
Denied
The Heart Valve Div. Medtronic Cardiovascular Surg has 4 FDA 510(k) cleared medical devices. Based in Minneapolis, US.
Historical record: 4 cleared submissions from 1991 to 1998. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by The Heart Valve Div. Medtronic Cardiovascular Surg Filter by specialty or product code using the sidebar.
5 devices
Cleared
Apr 30, 1998
DURAN FLEXIBLE ANNULOPLASTY RING MODEL NUMBER H608H
Cardiovascular
78d
Cleared
Aug 27, 1996
POSTERIOR ANNULOPLASTY BAND (MODEL 607)
Cardiovascular
215d
Cleared
Jul 14, 1995
UNIPOLAR PEDIATRIC TEMPORARY PACING LEAD, MODEL 6491
Cardiovascular
280d
Cleared
Nov 23, 1992
UNIPOLAR TEMPORARY MYOCARDIAL PACING WIRE, 6493
Cardiovascular
193d
Cleared
Nov 22, 1991
DURAN FLEX ANNULOPLASTY RING/OBTUR H601H, MODIFIED
Cardiovascular
38d