Introduction to FDA’s
Division of Neurological and
Physical Medicine Devices
AANS Abbreviated Slide Deck
Coming Soon
AANS FDA Session 2018
- Patients in the U.S. have access to high-quality, safe, and effective medical devices of public health importance first in the world.
- The U.S. is the world’s leader in regulatory science,
medical device innovation and manufacturing, and
radiation-emitting product safety. - U.S. post-market surveillance quickly identifies
poorly performing devices, accurately characterizes
real-world performance, and facilitates device
approval or clearance. - Devices are legally marketed in the U.S. and remain
safe, effective, and of high-quality. - Consumers, patients, their caregivers, and providers
have access to understandable science-based
information about medical devices and use this
information to make health care decisions.
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