This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
| Device | P090028S012 |
| Classification Name | None |
| Applicant | |
| PMA | P090028 |
| Supplement | S012 |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P090028 | Original Filing | |
| S018 | 2022-09-30 | Real-time Process |
| S017 | 2019-05-21 | 30-day Notice |
| S016 | 2018-10-16 | Normal 180 Day Track No User Fee |
| S015 | 2018-02-21 | Normal 180 Day Track No User Fee |
| S014 | 2018-02-12 | 30-day Notice |
| S013 | 2018-01-09 | Normal 180 Day Track No User Fee |
| S012 | ||
| S011 | 2017-09-25 | 30-day Notice |
| S010 | 2016-12-02 | Normal 180 Day Track |
| S009 | 2015-08-10 | 30-day Notice |
| S008 | 2015-06-25 | 30-day Notice |
| S007 | 2013-09-20 | 30-day Notice |
| S006 | 2012-11-29 | 30-day Notice |
| S005 | 2012-11-15 | 30-day Notice |
| S004 | 2012-10-17 | 30-day Notice |
| S003 | 2012-09-19 | 30-day Notice |
| S002 | 2012-03-22 | 30-day Notice |
| S001 | 2011-10-11 | 30-day Notice |
| Device ID | PMA | Supp |
|---|---|---|
| 10758750001453 | P090028 | 007 |
| 10758750001446 | P090028 | 007 |