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December 6, 2006
 Neurological Devices Panel of the Medical Devices Advisory
Committee; Notice of Meeting
On January 26, 2007, a U.S. Food and Drug Administration
committee will discuss and make recommendations on a
pre-market notification application for a device
intended for the treatment of major depressive disorder.
The committee will also hear and discuss post approval
study reports for two recently approved neurological
device pre-market approval applications. The agency
intends to make background available to the public no
later than one business day before the meeting.
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