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  4. March 21, 2019: Neurological Devices Panel of the Medical Devices Advisory Committee Meeting Announcement - 03/21/2019 - 03/21/2019
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Event Title
March 21, 2019: Neurological Devices Panel of the Medical Devices Advisory Committee Meeting Announcement
March 21, 2019


Date:
March 21, 2019
Time:
08:00 AM - 05:00 PM EDT

Center Date Time Location
CDRH March 21, 2019 8:00 a.m. - 5:00 p.m. Hilton Washington, DC North/Gaithersburg
Salons A, B, C, and D
620 Perry Pkwy.
Gaithersburg, MD 20877
301–977–8900

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. FDA-2019-N-0176]

Neurological Devices Panel of the Medical Devices Advisory Committee; Notice of Meeting

AGENCY:  Food and Drug Administration, HHS.

ACTION:  Notice.

SUMMARY:  The Food and Drug Administration (FDA) announces a forthcoming public advisory committee meeting of the Neurological Devices Panel of the Medical Devices Advisory Committee.  The general function of the committee is to provide advice and recommendations to the Agency on FDA's regulatory issues.  The meeting will be open to the public.

DATES:  The meeting will be held on March 21, 2019, from 8 a.m. to 5 p.m.

ADDRESSES:  Hilton Washington, DC North/Gaithersburg, Salons A, B, C, and D, 620 Perry Pkwy., Gaithersburg, MD 20877.  The hotel's phone number is 301-977-8900; additional information available online at:  https://www3.hilton.com/en/hotels/maryland/hilton-washington-dc-north-gaithersburg-GAIGHHF/index.html?SEO_id=GMB-HI-GAIGHHF%20.  Answers to commonly asked questions including information regarding special accommodations due to a disability, visitor parking, and transportation may be accessed at:  https://www.fda.gov/AdvisoryCommittees/AboutAdvisoryCommittees/ucm408555.htm.

FOR FURTHER INFORMATION CONTACT:  Aden Asefa, Center for Devices and Radiological Health, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 66, Rm. G642, Silver Spring, MD 20993-0002, Aden.Asefa@fda.hhs.gov, 301-796-0400, or FDA Advisory Committee Information Line, 1-800-741-8138 (301-443-0572 in the Washington, DC area).  A notice in the Federal Register about last minute modifications that impact a previously announced advisory committee meeting cannot always be published quickly enough to provide timely notice.  Therefore, you should always check the Agency's website at https://www.fda.gov/AdvisoryCommittees/default.htm and scroll down to the appropriate advisory committee meeting link, or call the advisory committee information line to learn about possible modifications before coming to the meeting.

SUPPLEMENTARY INFORMATION:

Agenda:  On March 21, 2019, the committee will discuss and make recommendations on clinical information related to the de novo request for the NeuroAD Therapy System by Neuronix, Ltd.  The NeuroAD Therapy System is intended to provide concurrent neurostimulation and cognitive training for the treatment of mild to moderate Alzheimer's dementia.

FDA intends to make background material available to the public no later than 2 business days before the meeting.  If FDA is unable to post the background material on its website prior to the meeting, the background material will be made publicly available at the location of the advisory committee meeting, and the background material will be posted on FDA's website after the meeting.  Background material is available at https://www.fda.gov/AdvisoryCommittees/Calendar/default.htm.  Scroll down to the appropriate advisory committee meeting link.

Procedure:  Interested persons may present data, information, or views, orally or in writing, on issues pending before the committee.  Written submissions may be made to the contact person on or before March 1, 2019.  Oral presentations from the public will be scheduled on March 21, 2019, between approximately 1 p.m. and 2 p.m.  Those individuals interested in making formal oral presentations should notify the contact person and submit a brief statement of the general nature of the evidence or arguments they wish to present, the names and addresses of proposed participants, and an indication of the approximate time requested to make their presentation on or before February 21, 2019.  Time allotted for each presentation may be limited.  If the number of registrants requesting to speak is greater than can be reasonably accommodated during the scheduled open public hearing session, FDA may conduct a lottery to determine the speakers for the scheduled open public hearing session.  The contact person will notify interested persons regarding their request to speak by February 22, 2019. 

Persons attending FDA's advisory committee meetings are advised that the Agency is not responsible for providing access to electrical outlets.

FDA welcomes the attendance of the public at its advisory committee meetings and will make every effort to accommodate persons with disabilities.  If you require accommodations due to a disability, please contact AnnMarie Williams at Annmarie.Williams@fda.hhs.gov or 301-796-5966 at least 7 days in advance of the meeting.

FDA is committed to the orderly conduct of its advisory committee meetings.  Please visit our website at https://www.fda.gov/AdvisoryCommittees/AboutAdvisoryCommittees/ucm111462.htm for procedures on public conduct during advisory committee meetings.

Notice of this meeting is given under the Federal Advisory Committee Act (5 U.S.C. app. 2).

Dated: January 16, 2019.

Leslie Kux,

Associate Commissioner for Policy.

 


Meeting Materials

Title File Type/Size Source Organization
Neurological Devices Panel March 21, 2019 Agenda (57.22 KB) Neurological Devices Panel March 21, 2019 Agenda
Neurological Devices Panel March 21, 2019 Roster (87.37 KB) Neurological Devices Panel March 21, 2019 Roster
Neurological Devices Panel March 21, 2019 FDA Executive Summary Neurological Devices Panel March 21, 2019 FDA Executive Summary
Neurological Devices Panel March 21, 2019 24 Hour Summary (124.82 KB) Neurological Devices Panel March 21, 2019 24 Hour Summary
Neurological Devices Panel March 21, 2019 Panel Questions (147.21 KB) Neurological Devices Panel March 21, 2019 Panel Questions
Neurological Devices Panel March 21, 2019 FDA Presentation Neurological Devices Panel March 21, 2019 FDA Presentation
Neurological Devices Panel March 21, 2019 Sponsor Panel Pack Table of Contents (62.40 KB) Neurological Devices Panel March 21, 2019 Sponsor Panel Pack Table of Contents
Neurological Devices Panel March 21, 2019 Sponsor Executive Summary Neurological Devices Panel March 21, 2019 Sponsor Executive Summary
Neurological Devices Panel March 21, 2019 Appendix 1 - Pivotal Study Protocol (539.19 KB) Neurological Devices Panel March 21, 2019 Appendix 1 - Pivotal Study Protocol
Neurological Devices Panel March 21, 2019 Appendix 2 - ADAS-Cog Administration and Scoring Manual (907.11 KB) Neurological Devices Panel March 21, 2019 Appendix 2 - ADAS-Cog Administration and Scoring Manual
Neurological Devices Panel March 21, 2019 Appendix 3 - ADCS-CGIC Scale (Report Forms) Neurological Devices Panel March 21, 2019 Appendix 3 - ADCS-CGIC Scale (Report Forms)
Neurological Devices Panel March 21, 2019 Appendix 4 - Physician Survey Report (694.41 KB) Neurological Devices Panel March 21, 2019 Appendix 4 - Physician Survey Report
Neurological Devices Panel March 21, 2019 Appendix 5 - Patient Case Example Videos (12.62 KB) Neurological Devices Panel March 21, 2019 Appendix 5 - Patient Case Example Videos
Neurological Devices Panel March 21, 2019 Sponsor Presentation Neurological Devices Panel March 21, 2019 Sponsor Presentation
Neurological Devices Panel March 21, 2019 Video 2 - Eileen Brannigan (41.48 KB) Neurological Devices Panel March 21, 2019 Video 2 - Eileen Brannigan
Neurological Devices Panel March 21, 2019 Transcript Neurological Devices Panel March 21, 2019 Transcript

FDA Advisory Committee Information Line
1-800-741-8138
(301-443-0572 in the Washington DC area)

Please call the Information Line for up-to-date information on this meeting.

A notice in the Federal Register about last minute modifications that impact a previously announced advisory committee meeting cannot always be published quickly enough to provide timely notice. Therefore, you should always check the agency’s Web site and call the FDA Advisory Committee Information Line to learn about possible modifications before coming to the meeting.

Persons attending FDA’s advisory committee meetings are advised that the agency is not responsible for providing access to electrical outlets. FDA welcomes the attendance of the public at its advisory committee meetings and will make every effort to accommodate persons with disabilities. If you require accommodations due to a disability, please contact Lauren Tesh at (301) 796-9001 at least 7 days in advance of the meeting.

Answers to commonly asked questions including information regarding special accommodations due to a disability may be accessed at: Common Questions and Answers about FDA Advisory Committee Meetings.

FDA is committed to the orderly conduct of its advisory committee meetings. Please visit our Web site at Public Conduct During FDA Advisory Committee Meetings for procedures on public conduct during advisory committee meetings.

Notice of this meeting is given under the Federal Advisory Committee Act (5 U.S.C. app.2).