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2016-10-04
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Center for Devices and Radiological Health Veteran Amputee Devices; Public Workshop; Request for Comments
Notices
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D09002ee1c1dbe822
United States
Department of Health and Human Services
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United States Government Agency or Subagency
United States
Food and Drug Administration
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United States Government Agency or Subagency
The Food and Drug Administration (FDA) is announcing the following public workshop entitled ``Center for Devices and Radiological Health Veteran Amputee Devices.'' The purpose of this workshop is to engage all stakeholders involved in the research, development, and marketing of prosthetic limb medical devices used by veteran amputees. A specific goal is to engage veteran amputees who use prosthetic limb medical devices and hear their views on these devices so that these perspectives may be considered in the total product life cycle of prosthetic limb devices.
81 FR 68422
https://www.govinfo.gov/app/details/FR-2016-10-04/2016-23924
2016-23924
fr04oc16-53
4164-01-P
Docket No. FDA-2016-N-2655
https://www.govinfo.gov/app/details/FR-2016-10-04/2016-23924
https://www.govinfo.gov/content/pkg/FR-2016-10-04/html/2016-23924.htm
https://www.govinfo.gov/content/pkg/FR-2016-10-04/pdf/2016-23924.pdf
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81 FR 68422
Center for Devices and Radiological Health Veteran Amputee Devices; Public Workshop; Request for Comments; Federal Register Vol. 81, Issue
NOTICE
2016-23924
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
2016-11-30
Docket No. FDA-2016-N-2655
4164-01-P
2016-23924
Notice of public workshop; request for comments.
The Food and Drug Administration (FDA) is announcing the following public workshop entitled ``Center for Devices and Radiological Health Veteran Amputee Devices.'' The purpose of this workshop is to engage all stakeholders involved in the research, development, and marketing of prosthetic limb medical devices used by veteran amputees. A specific goal is to engage veteran amputees who use prosthetic limb medical devices and hear their views on these devices so that these perspectives may be considered in the total product life cycle of prosthetic limb devices.
The public workshop will be held on October 31, 2016, from 9 a.m. to 4 p.m. Submit either electronic or written comments on the public workshop by November 30, 2016.
Fabienne Santel, Center for Devices and Radiological Health, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 66, Rm. 3502, Silver Spring, MD 20993, 301-796- 9644, email: Fabienne.santel@fda.hhs.gov.
Meetings:
Center for Devices and Radiological Health Veteran Amputee Devices; Public Workshop
,
Fabienne.santel@fda.hhs.gov
Susan.Monahan@fda.hhs.gov
http://www.adobe.com/go/connectpro_overview
http://www.fda.gov
http://www.fda.gov/AboutFDA/WorkingatFDA/BuildingsandFacilities/WhiteOakCampusInformation/ucm241740.htm
http://www.fda.gov/MedicalDevices/NewsEvents/WorkshopsConferences/default.htm
http://www.fda.gov/regulatoryinformation/dockets/default.htm
http://www.regulations.gov
https://collaboration.fda.gov/common/help/en/support/meeting_test.htm
Federal Register
Vol. 81, no. 192
Office of the Federal Register, National Archives and Records Administration
2016-10-04
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https://www.govinfo.gov/app/details/FR-2016-10-04
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https://www.govinfo.gov/content/pkg/FR-2016-10-04/pdf/FR-2016-10-04.pdf
https://www.govinfo.gov/content/pkg/FR-2016-10-04/xml/FR-2016-10-04.xml
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