This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
Device | P200015S018 |
Classification Name | None |
Applicant | |
PMA | P200015 |
Supplement | S018 |
Supplement Number | Date | Supplement Type |
---|---|---|
P200015 | Original Filing | |
S032 | 2022-11-14 | 30-day Notice |
S031 | 2022-10-25 | 30-day Notice |
S030 | 2022-10-04 | 30-day Notice |
S029 | ||
S028 | ||
S027 | 2022-08-25 | 30-day Notice |
S026 | ||
S025 | ||
S024 | ||
S023 | 2022-06-30 | 30-day Notice |
S022 | 2022-06-06 | 30-day Notice |
S021 | 2022-05-25 | Normal 180 Day Track No User Fee |
S020 | ||
S019 | 2022-04-04 | 30-day Notice |
S018 | ||
S017 | 2022-01-14 | 30-day Notice |
S016 | 2021-11-03 | Normal 180 Day Track No User Fee |
S015 | 2021-10-19 | 30-day Notice |
S014 | 2021-09-30 | 30-day Notice |
S013 | 2021-08-30 | 30-day Notice |
S012 | 2021-08-25 | 30-day Notice |
S011 | ||
S010 | 2021-06-07 | Normal 180 Day Track No User Fee |
S009 | 2021-03-19 | Normal 180 Day Track No User Fee |
S008 | 2021-02-22 | 30-day Notice |
S007 | 2020-12-17 | 30-day Notice |
S006 | 2020-12-03 | 30-day Notice |
S005 | ||
S004 | 2020-09-08 | 30-day Notice |
S003 | 2020-11-17 | 30-day Notice |
S002 | 2020-11-02 | 30-day Notice |
S001 |
Device ID | PMA | Supp |
---|---|---|
00690103210866 | P200015 | 011 |
00690103210873 | P200015 | 011 |