This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
Device | P990043S026 |
Classification Name | None |
Applicant | |
PMA | P990043 |
Supplement | S026 |
Supplement Number | Date | Supplement Type |
---|---|---|
P990043 | Original Filing | |
S032 | 2021-11-23 | 30-day Notice |
S031 | 2020-07-16 | 30-day Notice |
S030 | 2019-08-28 | 30-day Notice |
S029 | 2019-06-18 | 30-day Notice |
S028 | 2018-05-30 | 30-day Notice |
S027 | 2018-03-30 | 30-day Notice |
S026 | ||
S025 | 2018-02-14 | 30-day Notice |
S024 | 2017-09-18 | 30-day Notice |
S023 | 2017-04-25 | 30-day Notice |
S022 | 2017-03-29 | 30-day Notice |
S021 | 2016-05-10 | 30-day Notice |
S020 | 2014-06-05 | 30-day Notice |
S019 | 2013-12-27 | 30-day Notice |
S018 | 2013-06-05 | 30-day Notice |
S017 | 2012-11-09 | Special (immediate Track) |
S016 | ||
S015 | 2012-02-17 | 30-day Notice |
S014 | 2011-08-18 | 30-day Notice |
S013 | 2009-11-13 | 135 Review Track For 30-day Notice |
S012 | 2009-11-13 | Real-time Process |
S011 | 2009-01-29 | 30-day Notice |
S010 | 2006-12-29 | 30-day Notice |
S009 | 2005-06-03 | 30-day Notice |
S008 | ||
S007 | 2004-04-05 | 30-day Notice |
S006 | 2004-03-11 | 30-day Notice |
S005 | 2004-01-30 | Special (immediate Track) |
S004 | 2003-04-10 | Normal 180 Day Track No User Fee |
S003 | 2002-10-17 | 30-day Notice |
S002 | 2002-01-22 | Normal 180 Day Track |
S001 |