[Federal Register Volume 79, Number 41 (Monday, March 3, 2014)]
[Notices]
[Pages 11796-11797]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2014-04522]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. FDA-2014-N-0001]


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

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice.

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    This notice announces a forthcoming meeting of a public advisory 
committee of the Food and Drug Administration (FDA). The meeting will 
be open to the public. The meeting of the Ophthalmic Devices Panel 
Advisory Committee scheduled for February 14, 2014, was postponed due 
to unanticipated weather conditions and rescheduled for March 14, 2014.
    Name of Committee: Ophthalmic Devices Panel of the Medical Devices 
Advisory Committee.
    General Function of the Committee: To provide advice and 
recommendations to the Agency on FDA's regulatory issues.
    Date and Time: The meeting will be held on March 14, 2014, from 8 
a.m. to 6 p.m. This meeting is being rescheduled because of a postponed 
meeting announced in the Federal Register of December 24, 2013 (78 FR 
77688), originally scheduled for February 14, 2014.
    Location: Hilton Washington, DC/North, 620 Perry Pkwy., 
Gaithersburg, MD 20877. The hotel's phone number is 301-977-8900.
    Contact Person: Natasha Facey, Center for Devices and Radiological 
Health, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 
66, rm. 1544, Silver Spring, MD 20933, 301-796-5920, 
[email protected], 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 Web site at http://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.
    Agenda: On March 14, 2014, the committee will discuss, make 
recommendations, and vote on information regarding the premarket 
approval application for the Visian Toric Implantable Collamer Lens 
(TICL) sponsored by STAAR Surgical Company. ``Visian TICL proposed 
indications for use:
     For adults 21-45 years of age;
     For correction of myopic astigmatism in adults with 
spherical equivalent ranging from -3.0D to <=-15.0D with cylinder of 
1.0D to 4.0D;
     For the reduction of myopic astigmatism in adults with 
spherical equivalent ranging from greater than -15.0D to -20.0D with 
cylinder 1.0D to 4.0D;
     With an anterior chamber depth (ACD) of 3.0 mm or greater, 
when measured from the corneal endothelium to the anterior surface of 
the crystalline lens and a stable refractive history (within 0.5 
Diopter for 1 year prior to implantation); and
     The Visian TICL is intended for placement in the posterior 
chamber (ciliary sulcus) of the phakic eye.''
    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 Web site 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 Web site after the meeting. Background material is 
available at http://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

[[Page 11797]]

submissions may be made to the contact person on or before March 7, 
2014. Oral presentations from the public will be scheduled between 
approximately 1 p.m. and 2 p.m. on March 14, 2014. 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 27, 2014. 
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 March 3, 2014.
    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 
physical disabilities or special needs. If you require special 
accommodations due to a disability, please contact AnnMarie Williams at 
[email protected] 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 Web site at http://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: February 25, 2014.
Jill Hartzler Warner,
Acting Associate Commissioner for Special Medical Programs.
[FR Doc. 2014-04522 Filed 2-28-14; 8:45 am]
BILLING CODE 4160-01-P