Medtronic, Inc. - FDA 510(k) Cleared Devices
213
Total
212
Cleared
0
Denied
213 devices
Cleared
Aug 05, 2008
PIONEER PLUS CATHETER
Cardiovascular
40d
Cleared
Aug 01, 2008
INTERCEPTOR PLUS CORONARY FILTER SYSTEMS
Cardiovascular
231d
Cleared
May 07, 2008
U-CLIP UNI-FIRE, MODEL M65
General & Plastic Surgery
21d
Cleared
May 05, 2008
CARDIOBLATE 68000 GNERATOR, BP2 SURGICAL ABLATION DEVICE, LP SURGICAL...
Cardiovascular
70d
Cleared
Mar 13, 2008
MEDTRONIC PROFILE 3D ANNULOPLASTY RING, MODEL 680R
Cardiovascular
107d
Cleared
Nov 21, 2007
REVEAL XT
Cardiovascular
159d
Cleared
Nov 21, 2007
REVEAL DX INSERTABLE CARDIAC MONITOR, REVEAL PATIENT ASSISTANT, MODEL(S)...
Cardiovascular
156d
Cleared
Oct 31, 2007
GUARDWIRE TEMPORARY OCCLUSION AND ASPIRATION SYSTEM- CAROTID
Cardiovascular
7d
Cleared
Oct 05, 2007
PIONEER CATHETER
Radiology
63d
Cleared
Apr 26, 2007
MEROGEL INJECTABLE BIORESORBABLE STENT
Ear, Nose, Throat
27d
Cleared
Aug 16, 2006
MODEL 3875 1 X 8 SC TEST STIMULATION LEAD
Neurology
28d
Cleared
Feb 28, 2006
CARDIOBLATE SURGICAL ABLATION GENERATOR, MODEL 68000
General & Plastic Surgery
13d
Cleared
May 27, 1981
MODELS 5976/5977 PACEMAKER PULSE GENER
Cardiovascular
75d
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