This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
Device | P890057S016 |
Classification Name | None |
Applicant | |
PMA | P890057 |
Supplement | S016 |
Supplement Number | Date | Supplement Type |
---|---|---|
P890057 | Original Filing | |
S025 | 2022-04-25 | Real-time Process |
S024 | ||
S023 | ||
S022 | 2014-04-29 | 30-day Notice |
S021 | 2013-10-28 | 30-day Notice |
S020 | 2011-12-01 | 135 Review Track For 30-day Notice |
S019 | 2007-01-03 | Real-time Process |
S018 | 2004-12-20 | Real-time Process |
S017 | 2004-07-14 | Normal 180 Day Track No User Fee |
S016 | ||
S015 | 2001-08-09 | Normal 180 Day Track |
S014 | 2001-02-22 | Panel Track |
S013 | 1999-11-19 | Normal 180 Day Track |
S012 | ||
S011 | ||
S010 | 1997-07-03 | Normal 180 Day Track |
S009 | 1997-05-16 | Normal 180 Day Track |
S008 | 1997-01-03 | Normal 180 Day Track |
S007 | 1996-02-26 | Normal 180 Day Track |
S006 | ||
S005 | 1993-03-15 | Normal 180 Day Track |
S004 | 1993-02-09 | Normal 180 Day Track |
S003 | 1992-06-29 | Panel Track |
S002 | 1992-02-03 | Normal 180 Day Track |
S001 | 1991-04-04 | Normal 180 Day Track |