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U.S. Department of Health and Human Services

Premarket Approval (PMA)

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Note: this medical device record is a supplement. The device description may have changed. Be sure to look at the original PMA to get an up-to-date view of this device.
 
Trade NameMEDTRONIC ENTRUST MODELS D153ATG, D153DRG, D153VRC, D154ATG, D154DRG, D154VRC, MEDTRONIC MODEL 9987 APPLICATION SOFTWAR
Classification Nameimplantable cardioverter defibrillator (non-crt)
Generic Namedual chamber icds
ApplicantMEDTRONIC VASCULAR
PMA NumberP980016
Supplement NumberS046
Date Received01/12/2005
Decision Date06/14/2005
Product Code
LWS[ Registered Establishments with LWS ]
Advisory Committee Cardiovascular
Supplement Typenormal 180 day track
Supplement Reason change design/components/specifications - other
Expedited Review Granted? No
Combination Product No
Recalls CDRH Recalls
Approval Order Statement 
Approval for the medtronic entrust models d153atg, d153drg, d153vrc, d154atg, d154drg, d154vrc, medtronic model 9987 application software and the medtronic model 2696 incheck patient assistant are indicated for use in icd patients with atrial tachyarrhythmias, or who are at significant risk of developing atrial tachyarrhythmias. The entrust models d153drg, d153vrc and d154 drg are intended to provide ventricular antitachycardia pacing and ventricular defibrillation for automated treatment of life-threatening ventricular arrhythmias. The entrust models d153atg and d1534atg are intended to provide ventricular antitachycardia pacing and ventricular defibrillation for automated treatment of life threatening ventricular arrhythmias. In addition, the device is intended to provide pacing, cardioversion, and defibrillation for treatment of patients with: 1) symptomatic, drug-refractory atrial fibrillation and/or 2) life-threatening ventricular tachyarrhythmias. Atrial rhythm management features such as atrial rate stabilization (ars), atrial preference pacing (app) and post mode switch overdrive (pmop) are indicated for the suppression of atrial tachyarrhythmias in icd-indicated patients with atrial septal lead placement and one or more of the above icd indications. Notes: a) use of the device has not been demonstrated to decrease the morbidity related to atrial tachyarrhythmias. B) the effectiveness of high frequency burst pacing (atrial-50hz burst therapy) in terminating device classified atrial tachycardia (at) was found to be 17% , and in terminating device classified atrial fibrillation (af) was found to be 16. 85% in the vt/at population studied. C) the effectiveness of high frequency burst pacing (atrial-50hz burst therapy) in terminating device classified atrial tachycardia (at) was found to be 11. 7% , and in terminating device classified atrial fibrillation (af) was found to be 18. 2% in the af only population studied.
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