This medical device record is a pma supplement. A supplement may have changed the device description/function or indication from that approved in the original pma. Be sure to look at the original pma record for more information.
Addition of an alternate facility as a source or the akreos lens button and an alternate supplier of methyl methacrylate.
Device | AKREOS POSTERIOR CHAMBER INTRAOCULAR LENS |
Generic Name | Intraocular Lens |
Applicant | Bausch & Lomb, Inc. |
Date Received | 2011-05-09 |
Decision Date | 2011-06-08 |
PMA | P060022 |
Supplement | S011 |
Product Code | HQL |
Advisory Committee | Ophthalmic |
Supplement Type | 30-day Notice |
Supplement Reason | Process Change - Manufacturer/sterilizer/packager/supplier |
Expedited Review | No |
Combination Product | No |
Applicant Address | Bausch & Lomb, Inc. 50 Technology Drive irvine, CA 92618 |
Supplement Number | Date | Supplement Type |
---|---|---|
P060022 | Original Filing | |
S030 | 2022-08-16 | 30-day Notice |
S029 | 2021-12-22 | 30-day Notice |
S028 | 2020-12-04 | 30-day Notice |
S027 | ||
S026 | ||
S025 | 2019-12-23 | 30-day Notice |
S024 | 2018-07-10 | 30-day Notice |
S023 | 2016-06-03 | 30-day Notice |
S022 | 2015-09-11 | 135 Review Track For 30-day Notice |
S021 | 2015-02-18 | 30-day Notice |
S020 | 2014-12-08 | Real-time Process |
S019 | 2014-05-15 | 30-day Notice |
S018 | ||
S017 | 2013-06-10 | 30-day Notice |
S016 | 2013-04-15 | Real-time Process |
S015 | 2013-02-22 | 30-day Notice |
S014 | 2012-08-20 | 30-day Notice |
S013 | 2012-03-20 | Real-time Process |
S012 | 2011-06-21 | Normal 180 Day Track |
S011 | 2011-05-09 | 30-day Notice |
S010 | 2011-02-16 | Normal 180 Day Track No User Fee |
S009 | 2011-03-18 | 30-day Notice |
S008 | 2011-03-18 | 135 Review Track For 30-day Notice |
S007 | 2010-04-30 | 30-day Notice |
S006 | 2010-01-29 | Real-time Process |
S005 | 2009-08-25 | 30-day Notice |
S004 | 2009-03-06 | 30-day Notice |
S003 | ||
S002 | 2008-10-24 | Real-time Process |
S001 | 2008-10-20 | 30-day Notice |