This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
| Device | P140017S009 |
| Classification Name | None |
| Applicant | |
| PMA | P140017 |
| Supplement | S009 |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P140017 | Original Filing | |
| S023 | 2022-11-16 | 30-day Notice |
| S022 | 2022-07-20 | 30-day Notice |
| S021 | 2022-02-28 | 30-day Notice |
| S020 | 2022-01-27 | 30-day Notice |
| S019 | 2021-07-29 | 30-day Notice |
| S018 | ||
| S017 | 2019-10-01 | 30-day Notice |
| S016 | ||
| S015 | 2019-06-20 | 30-day Notice |
| S014 | 2018-11-13 | Normal 180 Day Track No User Fee |
| S013 | ||
| S012 | 2018-10-01 | 30-day Notice |
| S011 | 2018-09-26 | Real-time Process |
| S010 | 2017-12-01 | 30-day Notice |
| S009 | ||
| S008 | 2017-09-11 | 30-day Notice |
| S007 | 2017-04-19 | 30-day Notice |
| S006 | 2016-11-23 | Normal 180 Day Track No User Fee |
| S005 | 2016-09-01 | Panel Track |
| S004 | 2016-04-25 | Normal 180 Day Track |
| S003 | 2016-04-08 | 30-day Notice |
| S002 | 2016-03-23 | 30-day Notice |
| S001 | 2015-06-17 | 30-day Notice |
| Device ID | PMA | Supp |
|---|---|---|
| 00643169588455 | P140017 | 000 |
| 00643169588448 | P140017 | 000 |
| 00643169588431 | P140017 | 000 |
| 00643169588196 | P140017 | 000 |
| 00643169588189 | P140017 | 000 |
| 00643169713895 | P140017 | 004 |
| 00643169713901 | P140017 | 004 |
| 00643169713888 | P140017 | 004 |