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DTSTART;TZID=America/New_York:20261020T200000
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UID:10000084-1792526400-1792530000@www.aans.org
SUMMARY:FDA Medical Device User Fee Reauthorization and What It Means for Neurosurgery
DESCRIPTION:Event Description:\nJoin the AANS/CNS Washington Committee Drugs & Devices Subcommittee for a webinar examining the FDA’s Medical Device User Fee Amendments (MDUFA) and the impact of the upcoming reauthorization on neurosurgery.\n \nThis session will provide an overview of how MDUFA is funded\, how it supports medical device review\, and what to expect from the next reauthorization cycle. Experts from the FDA\, medical device industry\, and clinical community will discuss how the program influences device development and review\, with a focus on technologies neurosurgeons help develop and use.\n \nModerator:\nJoshua M. Rosenow\, MD\nChair\, Drugs & Devices Subcommittee\n \nFeatured Speakers:\n• Kathryn Capanna\, MBA\, Associate Director\, Office of Strategic Partnerships and Technology Innovation\, U.S. Food and Drug Administration\n• Cory N. Criss\, MD\, Chief Operating Officer\, Midwest Pediatric Device Consortium\n• David McMullen\, MD\, Head of Medical Affairs\, Neuralink\n\n \nREGISTER HERE\n \nShare:\n				Click to share on Link (Opens in new window)\n				Link\n			\n				Click to share on LinkedIn (Opens in new window)\n				LinkedIn\n			\n				Click to share on Facebook (Opens in new window)\n				Facebook\n			\n				Click to share on X (Opens in new window)\n				X
URL:https://www.aans.org/event/fda-medical-device-user-fee-reauthorization-and-what-it-means-for-neurosurgery/
CATEGORIES:AANS/CNS
ATTACH;FMTTYPE=image/png:https://www.aans.org/wp-content/uploads/2026/10/Webinar-image-10.20-1.png
LOCATION:https://www.aans.org/event/fda-medical-device-user-fee-reauthorization-and-what-it-means-for-neurosurgery/
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