Medical Devices; Neurological Devices; Clarification of Classification for Human Dura Mater; Technical Amendment
Information
Type
Rule
Regulated products
Medical Devices
Published
June 24, 2011
Last updated
June 24, 2011
Description
Document number 2011-15817. The Food and Drug Administration (FDA) is amending the device regulations to clarify the applicability of the device classification for human dura mater. This action is being taken to improve the accuracy of the regulations.
Tags
Organization
Country / Region
United States
License
Other (Public Domain)