This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
Device | P160022S016 |
Classification Name | None |
Applicant | |
PMA | P160022 |
Supplement | S016 |
Supplement Number | Date | Supplement Type |
---|---|---|
P160022 | Original Filing | |
S028 | 2021-04-23 | Normal 180 Day Track No User Fee |
S027 | 2021-03-15 | 30-day Notice |
S026 | 2021-02-24 | 30-day Notice |
S025 | 2020-12-21 | 30-day Notice |
S024 | 2020-12-17 | 30-day Notice |
S023 | 2020-11-24 | 30-day Notice |
S022 | 2020-09-16 | 30-day Notice |
S021 | 2020-09-14 | 30-day Notice |
S020 | ||
S019 | ||
S018 | 2020-05-29 | 30-day Notice |
S017 | ||
S016 | ||
S015 | ||
S014 | ||
S013 | ||
S012 | 2019-07-26 | 30-day Notice |
S011 | 2019-05-13 | Real-time Process |
S010 | 2019-04-08 | Real-time Process |
S009 | 2019-03-19 | 30-day Notice |
S008 | ||
S007 | 2018-08-10 | Real-time Process |
S006 | 2018-06-07 | Real-time Process |
S005 | 2018-06-07 | Real-time Process |
S004 | 2018-05-18 | Real-time Process |
S003 | 2018-04-30 | 30-day Notice |
S002 | 2018-04-30 | 30-day Notice |
S001 | 2018-01-16 | Real-time Process |