This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
| Device | P100042S006 |
| Classification Name | None |
| Applicant | |
| PMA | P100042 |
| Supplement | S006 |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P100042 | Original Filing | |
| S033 | 2022-01-19 | 30-day Notice |
| S032 | ||
| S031 | 2020-07-09 | 30-day Notice |
| S030 | 2020-05-14 | 30-day Notice |
| S029 | 2020-02-03 | 30-day Notice |
| S028 | 2019-12-23 | Real-time Process |
| S027 | ||
| S026 | 2019-08-21 | 30-day Notice |
| S025 | 2019-08-02 | 30-day Notice |
| S024 | ||
| S023 | 2019-03-27 | 30-day Notice |
| S022 | 2019-03-18 | Real-time Process |
| S021 | 2019-02-21 | 30-day Notice |
| S020 | 2018-12-31 | Real-time Process |
| S019 | 2018-08-31 | 30-day Notice |
| S018 | 2018-08-16 | 30-day Notice |
| S017 | 2018-03-15 | 30-day Notice |
| S016 | 2018-02-08 | 30-day Notice |
| S015 | 2017-12-20 | 30-day Notice |
| S014 | 2017-10-10 | 30-day Notice |
| S013 | 2017-09-01 | Normal 180 Day Track |
| S012 | 2017-03-17 | Real-time Process |
| S011 | 2016-08-15 | 30-day Notice |
| S010 | 2016-04-25 | 30-day Notice |
| S009 | 2015-10-16 | 30-day Notice |
| S008 | 2015-08-28 | 135 Review Track For 30-day Notice |
| S007 | 2015-08-12 | Normal 180 Day Track |
| S006 | ||
| S005 | 2015-03-04 | 30-day Notice |
| S004 | 2014-12-24 | Normal 180 Day Track No User Fee |
| S003 | 2014-06-09 | 30-day Notice |
| S002 | 2014-04-17 | Real-time Process |
| S001 | 2012-10-04 | Normal 180 Day Track |
| Device ID | PMA | Supp |
|---|---|---|
| 15420045500105 | P100042 | 001 |
| 15420045500099 | P100042 | 001 |
| 15420045500082 | P100042 | 001 |
| 15420045500075 | P100042 | 001 |
| 15420045500068 | P100042 | 001 |
| 15420045500051 | P100042 | 001 |