This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
Device | P800002S027 |
Classification Name | None |
Applicant | |
PMA | P800002 |
Supplement | S027 |
Supplement Number | Date | Supplement Type |
---|---|---|
P800002 | Original Filing | |
S028 | 2021-01-19 | 30-day Notice |
S027 | ||
S026 | 2020-02-28 | 30-day Notice |
S025 | 2019-05-20 | 30-day Notice |
S024 | 2018-12-03 | 30-day Notice |
S023 | 2018-06-28 | 30-day Notice |
S022 | 2017-03-27 | 135 Review Track For 30-day Notice |
S021 | 2014-05-30 | 30-day Notice |
S020 | 2013-12-11 | 30-day Notice |
S019 | 2013-06-24 | 30-day Notice |
S018 | 2011-12-22 | Special (immediate Track) |
S017 | 2011-09-02 | 30-day Notice |
S016 | 2009-03-20 | 30-day Notice |
S015 | 2005-09-08 | 30-day Notice |
S014 | 2004-10-04 | 30-day Notice |
S013 | 2003-06-11 | 30-day Notice |
S012 | 2001-05-23 | 30-day Notice |
S011 | 1998-07-21 | 30-day Notice |
S010 | 1993-12-02 | Normal 180 Day Track |
S009 | 1992-01-21 | Normal 180 Day Track |
S008 | 1991-10-16 | Normal 180 Day Track |
S007 | 1988-03-08 | Normal 180 Day Track |
S006 | ||
S005 | 1983-10-11 | |
S004 | 1983-08-30 | |
S003 | 1982-01-07 | |
S002 | 1981-01-27 | |
S001 | 1981-04-09 |
Device ID | PMA | Supp |
---|---|---|
10801741010474 | P800002 | 000 |
10801741010467 | P800002 | 000 |
10801741010450 | P800002 | 000 |
10801741010474 | P800002 | 001 |
10801741010467 | P800002 | 001 |
10801741010450 | P800002 | 001 |
10801741010498 | P800002 | 008 |
10801741010481 | P800002 | 008 |