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Medtronic, Inc.

211 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
U-CLIP UNI-FIRE, MODEL M65 (K081082)Medtronic, Inc.2008-05-07
CARDIOBLATE 68000 GNERATOR, BP2 SURGICAL ABLATION DEVICE, LP SURGICAL ABLATION DEVICE, GEMINI-SSURGICAL ABLATION DEVICE (K080509)Medtronic, Inc.2008-05-05
MEDTRONIC PROFILE 3D ANNULOPLASTY RING, MODEL 680R (K073324)Medtronic, Inc.2008-03-13
REVEAL XT; INSERTABLE CARDIAC MONITOR (MODEL 9529), PATIENT ASSISTANT (MODEL 9539) (K071641)Medtronic, Inc.2007-11-21
REVEAL DX INSERTABLE CARDIAC MONITOR, REVEAL PATIENT ASSISTANT, MODEL(S) 9528,9538 (K071655)Medtronic, Inc.2007-11-21
GUARDWIRE TEMPORARY OCCLUSION AND ASPIRATION SYSTEM- CAROTID (K072990)Medtronic, Inc.2007-10-31
PIONEER CATHETER (K072155)Medtronic, Inc.2007-10-05
MEROGEL INJECTABLE BIORESORBABLE STENT (K070886)Medtronic, Inc.2007-04-26
MODEL 3875 1 X 8 SC TEST STIMULATION LEAD (K062041)Medtronic, Inc.2006-08-16
CARDIOBLATE SURGICAL ABLATION GENERATOR, MODEL 68000; CARDIOBLATE BP2 SURGICAL ABLATION DEVICE, MODEL 60831; CARDIOBLAT (K060400)Medtronic, Inc.2006-02-28
MODELS 5976/5977 PACEMAKER PULSE GENER (K810677)Medtronic, Inc.1981-05-27
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