Medical Devices; Neurological Devices; Classification of Cranial Motion Measurement Device
Information
Type
Rule
Regulated products
Medical Devices
Published
July 28, 2017
Last updated
July 28, 2017
Description
Document number 2017-15895. The Food and Drug Administration (FDA or Agency) is classifying the cranial motion measurement device into class II (special controls). The special controls that will apply to the device are identified in this order and will be part of the codified language for the cranial motion measurement device's classification. The Agency is classifying the device into class II (special controls) in order to provide a reasonable assurance of safety and effectiveness of the device.
Tags
Organization
Country / Region
United States
License
Other (Public Domain)