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Federal Register / Vol. 71, No.

142 / Tuesday, July 25, 2006 / Notices 42097

Notice of this meeting is given under orally or in writing, on issues pending Date and Time: The meeting will be
the Federal Advisory Committee Act (5 before the committee. Written held on August 24, 2006, from 8 a.m. to
U.S.C. app. 2). submissions may be made to the contact 5 p.m., and on August 25, 2006, from 9
Dated: July 17, 2006. person on or before August 22, 2006. a.m. to 5 p.m.
Oral presentations from the public will Location: Holiday Inn, Walker/
Randall W. Lutter,
be scheduled between approximately Whetstone Rooms, Two Montgomery
Associate Commissioner for Policy and
Planning. 8:15 a.m. and 8:45 a.m., and between Village Ave., Gaithersburg, MD.
approximately 3:30 p.m. and 4 p.m. Contact Person: David Krause, Center
[FR Doc. E6–11772 Filed 7–24–06; 8:45 am] for Devices and Radiological Health
Time allotted for each presentation may
BILLING CODE 4160–01–S (HFZ–410), Food and Drug
be limited. Those desiring to make
formal oral presentations should notify Administration, 9200 Corporate Blvd.,
the contact person and submit a brief Rockville, MD 20850, 301–594–3090,
DEPARTMENT OF HEALTH AND ext. 141, or FDA Advisory Committee
HUMAN SERVICES statement of the general nature of the
evidence or arguments they wish to Information Line, 1–800–741–8138
Food and Drug Administration present, the names and addresses of (301–443–0572 in the Washington, DC
proposed participants, and an area), code 3014512519. Please call the
Obstetrics and Gynecology Devices indication of the approximate time Information Line for up-to-date
Panel of the Medical Devices Advisory requested to make their presentation on information on this meeting.
Committee; Notice of Meeting or before August 22, 2006. Agenda: On August 24, 2006, the
committee will discuss, make
AGENCY: Food and Drug Administration, Persons attending FDA’s advisory
recommendations, and vote on a
HHS. committee meetings are advised that the
premarket approval application (PMA)
ACTION: Notice. agency is not responsible for providing
for an injectable device intended for use
access to electrical outlets.
in the correction of lipoatrophy of the
This notice announces a forthcoming FDA welcomes the attendance of the face in HIV (human immunodeficiency
meeting of a public advisory committee public at its advisory committee virus) positive patients and a second
of the Food and Drug Administration meetings and will make every effort to PMA for the same device intended for
(FDA). The meeting will be open to the accommodate persons with physical use as a filler material to restore soft
public. disabilities or special needs. If you tissue facial contours such as nasolabial
Name of the Committee: Obstetrics require special accommodations due to folds. On August 25, 2006, the
and Gynecology Devices Panel of the a disability, please contact AnnMarie committee will discuss and make
Medical Devices Advisory Committee. Williams at least 7 days in advance of
General Function of the Committee: recommendations on the
the meeting at 301–827–7291. reclassification, to Class II, of a Class III
To provide advice and Notice of this meeting is given under
recommendations to the agency on medical device: Cyanoacrylate tissue
the Federal Advisory Committee Act (5 adhesive. Background information for
FDA’s regulatory issues. U.S.C. app. 2).
Date and Time: The meeting will be this meeting, including the agenda and
held on August 29, 2006, from 8 a.m. to Dated: July 17, 2006. questions for the committee, will be
5 p.m. Randall W. Lutter, available to the public 1 business day
Location: Hilton Washington DC Associate Commissioner for Policy and before the meeting on the Internet at
North/Gaithersburg, Montgomery Planning. http://www.fda.gov/cdrh/panel (click on
Ballroom, 620 Perry Pkwy., [FR Doc. E6–11773 Filed 7–24–06; 8:45 am] ‘‘Upcoming CDRH Advisory Panel/
Gaithersburg, MD 20877. Committee Meetings’’). Material for the
BILLING CODE 4160–01–S
Contact: Michael Bailey, Center for August 24 and 25 sessions will be
Devices and Radiological Health (HFZ– posted on August 23, 2006.
470), Food and Drug Administration, DEPARTMENT OF HEALTH AND Procedure: On August 24, 2006, from
9200 Corporate Blvd., Rockville, MD HUMAN SERVICES 8 a.m. to 5 p.m., and on August 25,
20850, 301–594–1180 or FDA Advisory 2006, from 9:30 a.m. to 5 p.m., the
Committee Information Hotline, 1–800– Food and Drug Administration meeting is open to the public. Interested
741–8138 (301–443–0572 in the persons may present data, information,
Washington, DC area), code General and Plastic Surgery Devices or views, orally or in writing, on issues
3014512524. Please call the Information Panel of the Medical Devices Advisory pending before the committee. Written
Line for up-to-date information on this Committee; Notice of Meeting submissions may be made to the contact
meeting. person on or before August 10, 2006. On
Agenda: The committee will discuss, AGENCY: Food and Drug Administration, August 24, 2006, oral presentations from
make recommendations, and vote on a HHS. the public will be scheduled between
premarket approval application for a ACTION: Notice. approximately 8:30 a.m. and 9 a.m.,
non-invasive device for use as a approximately 11:45 a.m. and 12:15
complement to clinical breast This notice announces a forthcoming p.m., approximately 1:45 p.m. and 2:15
examination in asymptomatic women meeting of a public advisory committee p.m., and approximately 3:45 p.m. and
between the ages of 30 to 39. of the Food and Drug Administration 4:15 p.m. On August 25, 2006, oral
Background information, including the (FDA). At least one portion of the presentations from the public will be
agenda and questions for the committee, meeting will be closed to the public. scheduled between approximately 11
will be available to the public one Name of Committee: General and a.m. and 12 noon. Time allotted for each
business day before the meeting on the Plastic Surgery Devices Panel of the presentation may be limited. Those
sroberts on PROD1PC70 with NOTICES

Internet at http://www.fda.gov/cdrh/ Medical Devices Advisory Committee. desiring to make formal oral
panel (click on ‘‘Upcoming CDRH General Function of the Committee: presentations should notify the contact
Advisory Panel/Committee Meetings’’). To provide advice and person and submit a brief statement of
Procedure: Interested persons may recommendations to the agency on the general nature of the evidence or
present data, information, or views, FDA’s regulatory issues. arguments they wish to present, the

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