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 |