This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
Device | P150013S012 |
Classification Name | None |
Applicant | |
PMA | P150013 |
Supplement | S012 |
Supplement Number | Date | Supplement Type |
---|---|---|
P150013 | Original Filing | |
S025 | 2022-08-08 | Real-time Process |
S024 | 2022-01-31 | Special (immediate Track) |
S023 | 2021-11-17 | Special (immediate Track) |
S022 | ||
S021 | 2020-08-31 | Normal 180 Day Track |
S020 | 2020-06-29 | Panel Track |
S019 | 2020-02-06 | Normal 180 Day Track No User Fee |
S018 | 2019-09-05 | Normal 180 Day Track No User Fee |
S017 | 2019-06-14 | Normal 180 Day Track |
S016 | 2019-02-25 | Panel Track |
S015 | 2019-02-15 | 30-day Notice |
S014 | ||
S013 | 2018-12-21 | 30-day Notice |
S012 | ||
S011 | 2018-06-25 | Panel Track |
S010 | 2018-03-12 | 30-day Notice |
S009 | 2018-01-29 | Panel Track |
S008 | 2017-12-26 | 30-day Notice |
S007 | 2017-09-21 | Normal 180 Day Track No User Fee |
S006 | 2017-04-19 | Panel Track |
S005 | 2017-04-17 | 30-day Notice |
S004 | 2016-12-27 | Real-time Process |
S003 | 2016-08-19 | Real-time Process |
S002 | 2016-06-28 | Real-time Process |
S001 | 2015-12-31 | Panel Track |
Device ID | PMA | Supp |
---|---|---|
05700571107300 | P150013 | 000 |
05700573003563 | P150013 | 000 |
05700571112755 | P150013 | 000 |