Medtronic Neurological is one of 25799 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medtronic Neurological - FDA 510(k) Cleared Devices
Recent clearances: PISCES Z QUAD LEAD MODEL, 3890, PISCES Z QUAD COMPACT LEAD MODEL, 3891, PISCES Z QUAD PLUS LEAD MODEL, 3892, GRIP LOCK ANCHOR, MODEL 411374
2
Total
2
Cleared
0
Denied
Medtronic Neurological has 2 FDA 510(k) cleared medical devices. Based in Minneapolis, US.
Historical record: 2 cleared submissions from 2001 to 2003. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Medtronic Neurological Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medtronic Neurological
2 devices