This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
| Device | P150037S012 |
| Classification Name | None |
| Applicant | |
| PMA | P150037 |
| Supplement | S012 |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P150037 | Original Filing | |
| S014 | 2019-12-20 | Normal 180 Day Track No User Fee |
| S013 | ||
| S012 | ||
| S011 | 2018-07-16 | 30-day Notice |
| S010 | 2018-06-25 | 30-day Notice |
| S009 | 2018-05-04 | 30-day Notice |
| S008 | 2017-09-25 | Normal 180 Day Track |
| S007 | 2017-07-27 | Normal 180 Day Track No User Fee |
| S006 | 2017-06-02 | Normal 180 Day Track No User Fee |
| S005 | 2017-04-20 | 30-day Notice |
| S004 | 2017-03-15 | 30-day Notice |
| S003 | 2016-11-03 | 30-day Notice |
| S002 | 2016-08-26 | Normal 180 Day Track No User Fee |
| S001 | 2016-08-24 | Normal 180 Day Track No User Fee |
| Device ID | PMA | Supp |
|---|---|---|
| 00380657540075 | P150037 | 008 |