COLLAMER ULTRAVIOLET ABSORBING POSTERIOR CHAMBER INTRAOCULAR LENS

Intraocular Lens

FDA Premarket Approval P990013

This medical device has supplements. The device description/function or indication may have changed. Be sure to look at the supplements to get an up-to-date information on device changes. The labeling included below is the version at time of approval of the original pma or panel track supplement and may not represent the most recent labeling.

Pre-market Approval Supplement Details

This device is indicated for the correction of aphakia in persons 60 years of age or older in whom a cataractous lens has been removed by phacoemulsification cataract extraction. The lens is to be implanted in the posterior chamber and in the capsular bag through a tear-free capsulorhexis (circular tear anterior capsulotomy).

DeviceCOLLAMER ULTRAVIOLET ABSORBING POSTERIOR CHAMBER INTRAOCULAR LENS
Classification NameIntraocular Lens
Generic NameIntraocular Lens
ApplicantSTARR SURGICAL CO.
Date Received1999-03-05
Decision Date2000-04-02
PMAP990013
SupplementS
Product CodeHQL
Docket Number00M-1230
Advisory CommitteeOphthalmic
Expedited ReviewNo
Combination Product No
Applicant Address STARR SURGICAL CO. 1911 Walker Ave. monrovia, CA 91016
Summary:Summary of Safety and Effectiveness
Labeling: Labeling
Approval Order: Approval Order

Supplemental Filings

Supplement NumberDateSupplement Type
P990013Original Filing
S041 2021-06-22 30-day Notice
S040 2020-03-03 30-day Notice
S039 2019-06-27 30-day Notice
S038 2019-04-22 Real-time Process
S037 2017-07-06 30-day Notice
S036 2017-07-03 30-day Notice
S035 2017-05-19 30-day Notice
S034 2017-03-13 30-day Notice
S033 2014-01-13 30-day Notice
S032
S031 2011-03-30 30-day Notice
S030 2010-12-14 30-day Notice
S029 2010-08-17 Special (immediate Track)
S028 2010-07-15 30-day Notice
S027 2010-06-25 30-day Notice
S026 2010-05-17 30-day Notice
S025 2009-02-09 30-day Notice
S024 2008-10-09 30-day Notice
S023 2008-08-04 30-day Notice
S022 2008-07-23 135 Review Track For 30-day Notice
S021 2008-06-06 30-day Notice
S020 2008-05-05 30-day Notice
S019 2008-04-25 30-day Notice
S018 2008-04-02 Normal 180 Day Track
S017 2008-03-28 30-day Notice
S016 2008-03-20 30-day Notice
S015 2008-02-22 30-day Notice
S014 2007-11-29 Real-time Process
S013 2007-05-04 Special (immediate Track)
S012 2007-02-26 30-day Notice
S011 2007-02-26 30-day Notice
S010 2007-02-23 30-day Notice
S009 2007-02-23 135 Review Track For 30-day Notice
S008 2007-02-22 30-day Notice
S007 2007-02-22 30-day Notice
S006 2007-02-22 30-day Notice
S005
S004 2004-05-24 Special (immediate Track)
S003 2001-07-06 30-day Notice
S002
S001 2000-07-24 Normal 180 Day Track

NIH GUDID Devices

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