This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
Device | P160045S017 |
Classification Name | None |
Applicant | |
PMA | P160045 |
Supplement | S017 |
Supplement Number | Date | Supplement Type |
---|---|---|
P160045 | Original Filing | |
S038 | 2022-08-05 | Normal 180 Day Track No User Fee |
S037 | 2022-06-14 | Real-time Process |
S036 | 2022-03-29 | 135 Review Track For 30-day Notice |
S035 | 2022-03-08 | Panel Track |
S034 | 2021-12-23 | Normal 180 Day Track No User Fee |
S033 | ||
S032 | ||
S031 | ||
S030 | 2021-05-14 | 30-day Notice |
S029 | ||
S028 | ||
S027 | ||
S026 | ||
S025 | ||
S024 | 2020-11-06 | 30-day Notice |
S023 | 2020-10-01 | 30-day Notice |
S022 | 2020-09-11 | 30-day Notice |
S021 | ||
S020 | 2020-05-14 | 30-day Notice |
S019 | ||
S018 | 2019-10-16 | 30-day Notice |
S017 | ||
S016 | 2019-07-22 | 30-day Notice |
S015 | 2019-04-23 | 30-day Notice |
S014 | 2019-01-31 | 30-day Notice |
S013 | 2019-01-25 | 30-day Notice |
S012 | 2018-11-13 | 30-day Notice |
S011 | 2018-10-19 | 30-day Notice |
S010 | 2018-10-09 | 30-day Notice |
S009 | ||
S008 | 2018-07-20 | 30-day Notice |
S007 | ||
S006 | 2018-05-02 | 30-day Notice |
S005 | 2018-03-22 | Normal 180 Day Track No User Fee |
S004 | ||
S003 | 2017-11-20 | 30-day Notice |
S002 | 2017-11-08 | 30-day Notice |
S001 | 2017-07-28 | 30-day Notice |
Device ID | PMA | Supp |
---|---|---|
10190302015103 | P160045 | 000 |
10190302006156 | P160045 | 000 |
10190302006095 | P160045 | 000 |
10190302006064 | P160045 | 000 |
10190302015646 | P160045 | 000 |
10190302006071 | P160045 | 000 |
10190302017756 | P160045 | 000 |