This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
Device | P080027S002 |
Classification Name | None |
Applicant | |
PMA | P080027 |
Supplement | S002 |
Supplement Number | Date | Supplement Type |
---|---|---|
P080027 | Original Filing | |
S039 | 2021-03-25 | 30-day Notice |
S038 | 2021-02-01 | 30-day Notice |
S037 | 2020-09-14 | 30-day Notice |
S036 | ||
S035 | 2019-08-16 | 30-day Notice |
S034 | 2018-11-07 | 30-day Notice |
S033 | 2018-03-13 | 30-day Notice |
S032 | 2018-01-08 | 30-day Notice |
S031 | 2017-12-08 | 30-day Notice |
S030 | 2017-09-14 | 30-day Notice |
S029 | 2017-08-14 | 30-day Notice |
S028 | 2017-06-07 | 30-day Notice |
S027 | 2017-04-14 | 30-day Notice |
S026 | 2017-01-30 | 30-day Notice |
S025 | 2016-11-28 | 30-day Notice |
S024 | 2016-10-24 | 30-day Notice |
S023 | 2016-04-15 | 30-day Notice |
S022 | 2016-02-01 | 30-day Notice |
S021 | 2015-09-03 | 30-day Notice |
S020 | ||
S019 | 2014-12-23 | 30-day Notice |
S018 | 2014-09-03 | Special (immediate Track) |
S017 | 2014-06-06 | Real-time Process |
S016 | 2014-03-04 | Normal 180 Day Track |
S015 | 2013-11-19 | 30-day Notice |
S014 | 2013-09-06 | 30-day Notice |
S013 | 2013-08-28 | 30-day Notice |
S012 | 2013-07-12 | Special (immediate Track) |
S011 | 2013-04-29 | Special (immediate Track) |
S010 | 2013-02-21 | 30-day Notice |
S009 | 2013-02-19 | Special (immediate Track) |
S008 | 2012-12-28 | 30-day Notice |
S007 | 2012-11-28 | Special (immediate Track) |
S006 | 2011-04-06 | 30-day Notice |
S005 | 2011-03-16 | 135 Review Track For 30-day Notice |
S004 | ||
S003 | 2011-02-23 | 135 Review Track For 30-day Notice |
S002 | ||
S001 | 2010-08-03 | Panel Track |
Device ID | PMA | Supp |
---|---|---|
00608337000542 | P080027 | 001 |
20608337000539 | P080027 | 001 |