This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
Device | P090031S005 |
Classification Name | None |
Applicant | |
PMA | P090031 |
Supplement | S005 |
Supplement Number | Date | Supplement Type |
---|---|---|
P090031 | Original Filing | |
S015 | 2022-10-12 | 30-day Notice |
S014 | 2022-10-03 | 30-day Notice |
S013 | 2022-06-17 | 30-day Notice |
S012 | 2021-09-15 | 30-day Notice |
S011 | 2021-09-15 | 30-day Notice |
S010 | 2021-08-11 | 30-day Notice |
S009 | 2019-07-19 | Normal 180 Day Track |
S008 | 2017-05-23 | Real-time Process |
S007 | 2016-08-24 | 30-day Notice |
S006 | 2016-02-10 | Special (immediate Track) |
S005 | ||
S004 | 2014-12-24 | 135 Review Track For 30-day Notice |
S003 | 2014-11-07 | Real-time Process |
S002 | 2014-06-10 | 30-day Notice |
S001 | 2014-05-08 | 30-day Notice |
Device ID | PMA | Supp |
---|---|---|
05060548950033 | P090031 | 000 |
05060459970090 | P090031 | 000 |
08437027710018 | P090031 | 000 |