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FDA approves Medtronic's new pacemaker system:

This article was originally published in Clinica

Executive Summary

The Medtronic Kappa 700 implantable pacing series has received premarket approval from the US FDA. The Minneapolis, Minnesota-based company says its new series of pacemaker systems is able to detect and respond to atrial arrhythmias with appropriate pacing within seconds. Other features of the series include the Remote Assistant, a hand-held monitor which allows patients to check the status of their pacing leads and pacemakers, and Medtronic.Vision software which provides doctors with patient demographics, test results and diagnostic data.

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