This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
Device | P080010S019 |
Classification Name | None |
Applicant | |
PMA | P080010 |
Supplement | S019 |
Supplement Number | Date | Supplement Type |
---|---|---|
P080010 | Original Filing | |
S021 | 2022-11-09 | 30-day Notice |
S020 | 2020-12-10 | 30-day Notice |
S019 | ||
S018 | 2019-02-26 | 30-day Notice |
S017 | 2018-12-21 | 30-day Notice |
S016 | 2018-12-21 | 30-day Notice |
S015 | 2018-04-11 | 30-day Notice |
S014 | 2017-09-28 | 30-day Notice |
S013 | 2016-06-01 | 30-day Notice |
S012 | 2015-12-18 | 30-day Notice |
S011 | 2015-06-26 | 30-day Notice |
S010 | 2013-11-26 | 30-day Notice |
S009 | 2013-05-24 | 30-day Notice |
S008 | 2012-04-23 | 30-day Notice |
S007 | 2012-01-30 | 30-day Notice |
S006 | ||
S005 | 2010-04-01 | 30-day Notice |
S004 | 2009-06-30 | 30-day Notice |
S003 | 2009-06-09 | 30-day Notice |
S002 | 2009-04-28 | Normal 180 Day Track No User Fee |
S001 | 2009-01-27 | Normal 180 Day Track |