This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
| Device | P120011S014 |
| Classification Name | None |
| Applicant | |
| PMA | P120011 |
| Supplement | S014 |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P120011 | Original Filing | |
| S024 | 2021-12-22 | 30-day Notice |
| S023 | ||
| S022 | 2021-05-27 | Normal 180 Day Track No User Fee |
| S021 | 2020-11-03 | 135 Review Track For 30-day Notice |
| S020 | 2020-07-02 | 30-day Notice |
| S019 | ||
| S018 | 2020-03-17 | 30-day Notice |
| S017 | ||
| S016 | 2019-06-21 | 30-day Notice |
| S015 | ||
| S014 | ||
| S013 | 2018-07-25 | 30-day Notice |
| S012 | 2018-06-11 | Real-time Process |
| S011 | 2018-06-08 | 30-day Notice |
| S010 | 2017-10-23 | Special (immediate Track) |
| S009 | 2017-10-05 | Normal 180 Day Track No User Fee |
| S008 | 2016-10-04 | 30-day Notice |
| S007 | 2016-09-21 | 30-day Notice |
| S006 | 2016-07-28 | Normal 180 Day Track No User Fee |
| S005 | 2016-04-15 | 30-day Notice |
| S004 | 2016-04-15 | 30-day Notice |
| S003 | 2016-03-28 | 135 Review Track For 30-day Notice |
| S002 | 2015-11-04 | Normal 180 Day Track No User Fee |
| S001 | 2015-07-24 | 30-day Notice |
| Device ID | PMA | Supp |
|---|---|---|
| 00850034511931 | P120011 | 000 |
| 00850034511337 | P120011 | 000 |
| 00850034511399 | P120011 | 000 |
| 00850034511627 | P120011 | 000 |
| 00850034511658 | P120011 | 000 |
| 00850034511672 | P120011 | 000 |
| 00850034511757 | P120011 | 000 |
| 00850034511771 | P120011 | 000 |
| 00850034511801 | P120011 | 000 |
| 00850034511825 | P120011 | 000 |
| 00850034511863 | P120011 | 000 |
| 00850034511894 | P120011 | 000 |
| 00850034511924 | P120011 | 000 |
| 00850034511153 | P120011 | 000 |