US FDA's Neurological Devices Advisory Panel convened March 1 in Gaithersburg, Md., to discuss and give recommendations to the agency on what should be required of sponsors when conducting clinical trials for intracranial aneurysm devices and making product submissions. Also see "Brain Trust Advises US FDA On Aneurysm Device Trials" - Medtech Insight, 2 March, 2018.
At the end of the meeting, Christopher Loftus, chief medical officer in the Division of Neurological and Physical Medicine Devices...