This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
Device | P150029S032 |
Classification Name | None |
Applicant | |
PMA | P150029 |
Supplement | S032 |
Supplement Number | Date | Supplement Type |
---|---|---|
P150029 | Original Filing | |
S038 | 2022-04-01 | 30-day Notice |
S037 | 2021-11-17 | Special (immediate Track) |
S036 | 2021-01-27 | Special (immediate Track) |
S035 | 2020-11-03 | 30-day Notice |
S034 | 2019-11-29 | 30-day Notice |
S033 | 2019-10-17 | 30-day Notice |
S032 | ||
S031 | 2019-08-21 | 30-day Notice |
S030 | 2019-07-15 | 30-day Notice |
S029 | 2019-06-19 | 30-day Notice |
S028 | ||
S027 | 2019-02-11 | 30-day Notice |
S026 | 2019-02-01 | 30-day Notice |
S025 | 2018-11-07 | 30-day Notice |
S024 | 2018-11-07 | 30-day Notice |
S023 | 2018-11-02 | 30-day Notice |
S022 | 2018-10-15 | 30-day Notice |
S021 | 2018-07-09 | 30-day Notice |
S020 | 2018-06-19 | 30-day Notice |
S019 | 2018-06-07 | Special (immediate Track) |
S018 | 2018-03-26 | 30-day Notice |
S017 | 2018-03-12 | 30-day Notice |
S016 | 2018-02-09 | Real-time Process |
S015 | 2018-02-07 | 30-day Notice |
S014 | 2017-12-22 | 30-day Notice |
S013 | 2017-11-24 | 30-day Notice |
S012 | 2017-10-30 | 30-day Notice |
S011 | 2017-07-17 | 30-day Notice |
S010 | 2017-06-22 | Real-time Process |
S009 | 2017-05-30 | 30-day Notice |
S008 | 2017-03-31 | 30-day Notice |
S007 | ||
S006 | 2016-12-23 | Real-time Process |
S005 | 2016-12-12 | 30-day Notice |
S004 | 2016-11-28 | 30-day Notice |
S003 | 2016-11-28 | 30-day Notice |
S002 | 2016-11-02 | 30-day Notice |
S001 | 2016-07-21 | 30-day Notice |
Device ID | PMA | Supp |
---|---|---|
00763000049492 | P150029 | 000 |
00643169938076 | P150029 | 010 |
00763000049997 | P150029 | 010 |
00763000049492 | P150029 | 010 |