This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
Device | P830063S018 |
Classification Name | None |
Applicant | |
PMA | P830063 |
Supplement | S018 |
Supplement Number | Date | Supplement Type |
---|---|---|
P830063 | Original Filing | |
S024 | 2022-10-18 | 30-day Notice |
S023 | 2022-03-29 | 30-day Notice |
S022 | 2022-03-02 | 30-day Notice |
S021 | ||
S020 | 2021-11-09 | Real-time Process |
S019 | 2021-05-26 | 30-day Notice |
S018 | ||
S017 | 2020-07-29 | 30-day Notice |
S016 | 2020-03-05 | Real-time Process |
S015 | 2020-02-24 | Special (immediate Track) |
S014 | 2019-11-15 | 30-day Notice |
S013 | ||
S012 | 2019-06-27 | Real-time Process |
S011 | ||
S010 | 2017-10-26 | 30-day Notice |
S009 | 2016-12-02 | 30-day Notice |
S008 | 2015-10-13 | Special (immediate Track) |
S007 | 2015-05-29 | 30-day Notice |
S006 | 2007-10-09 | Real-time Process |
S005 | 2006-11-24 | Normal 180 Day Track |
S004 | 2001-11-13 | Normal 180 Day Track |
S003 | 2000-10-31 | Real-time Process |
S002 | 2000-01-18 | Normal 180 Day Track |
S001 | 1995-07-06 | Normal 180 Day Track |
Device ID | PMA | Supp |
---|---|---|
07332414111038 | P830063 | 006 |