Another Advisory Panel For Watchman Yields Another Mixed Result
This article was originally published in The Gray Sheet
Executive Summary
The market prospects for Boston Scientific’s Watchman left-atrial appendage closure device for stroke remain uncertain following a narrow vote in favor of the device’s risk-benefit profile by FDA’s Circulatory System Devices Advisory Panel even though a majority of the panel did not believe the clinical data proved the device is effective.
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Boston Sci’s Watchman Stroke Device Finally Lands FDA Approval, With Favorable Labeling
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