The United States Food and Drug Administration (FDA) ensures that patients in the U.S. have access to safe and effective medical devices. The Division of Neurological and Physical Medicine Devices reviews medical technologies that interface with the nervous system. This article addresses how to navigate the FDA's regulatory landscape to successfully bring medical devices to patients.
|Original language||English (US)|
|Number of pages||6|
|State||Published - Dec 7 2016|
ASJC Scopus subject areas