Medtronic Vascular - FDA 510(k) Cleared Devices
475
Total
453
Cleared
0
Denied
FDA 510(k) cleared devices by Medtronic Vascular Neurology ✕
89 devices
Cleared
Aug 12, 2004
POLYGRAM NET BIOFEEDBACK APPLICATION
Neurology
93d
Cleared
Mar 25, 2004
POLYETHER URETHANE MATERIAL CHANGE IN NEUROSTIMULATION LEADS
Neurology
21d
Cleared
Sep 11, 2003
RESUME II LEAD KIT FOR SPINAL CORD STIMULATION (SCS) AND PERIPHERAL NERVE...
Neurology
22d
Cleared
Aug 01, 2001
MEDTRONIC MODEL 7495LZ LOW IMPEDANCE EXTENSION
Neurology
181d
Cleared
Jun 22, 2001
MEDTRONIC SPINAL CORD STIMULATION AND PERIPHERAL NERVE STIMULATION SYSTEMS...
Neurology
30d
Cleared
Apr 28, 2000
MEDTRONIC MODEL 7499 EXTENSION
Neurology
78d
Cleared
Apr 12, 2000
MEDTRONIC EXTENSION PASSER TUNNELING SYSTEM (38 CM), MODEL 3555-38
Neurology
89d
Cleared
Feb 09, 1999
MEDTRONIC MODEL 7495 EXTENSION KIT
Neurology
28d
Cleared
Nov 10, 1998
PERIPHERAL NERVE STIMULATION
Neurology
88d
Cleared
Feb 06, 1998
MEDTRONIC TWIST LOCK ANCHOR (PARTNUMBER 103953/3550TLA)
Neurology
184d
Cleared
Feb 03, 1998
MEDTRONIC MODEL 3998 LEAD
Neurology
267d
Cleared
Aug 22, 1997
MEDTRONIC MODEL 3273/3274 RF RECEIVER AND MODEL 3629/3630 SCREENER
Neurology
81d
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