This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
| Device | P100031S022 |
| Classification Name | None |
| Applicant | |
| PMA | P100031 |
| Supplement | S022 |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P100031 | Original Filing | |
| S027 | 2021-09-30 | Normal 180 Day Track |
| S026 | 2018-10-26 | Normal 180 Day Track No User Fee |
| S025 | 2018-10-09 | 30-day Notice |
| S024 | 2018-04-17 | Real-time Process |
| S023 | 2018-03-01 | Real-time Process |
| S022 | ||
| S021 | 2017-10-11 | Real-time Process |
| S020 | 2017-09-28 | Normal 180 Day Track |
| S019 | 2017-08-03 | 30-day Notice |
| S018 | 2017-05-24 | 30-day Notice |
| S017 | 2017-02-21 | Normal 180 Day Track |
| S016 | 2016-02-16 | 30-day Notice |
| S015 | 2016-01-27 | 30-day Notice |
| S014 | 2016-01-27 | 135 Review Track For 30-day Notice |
| S013 | 2015-10-07 | 30-day Notice |
| S012 | 2014-10-16 | Real-time Process |
| S011 | 2014-04-04 | Real-time Process |
| S010 | 2012-11-30 | 30-day Notice |
| S009 | 2012-09-04 | Normal 180 Day Track |
| S008 | 2012-09-04 | Normal 180 Day Track |
| S007 | ||
| S006 | 2012-02-29 | 30-day Notice |
| S005 | 2012-01-31 | 135 Review Track For 30-day Notice |
| S004 | 2011-08-29 | 135 Review Track For 30-day Notice |
| S003 | 2011-08-17 | Normal 180 Day Track No User Fee |
| S002 | 2011-08-17 | 135 Review Track For 30-day Notice |
| S001 | 2011-07-01 | 30-day Notice |
| Device ID | PMA | Supp |
|---|---|---|
| 07613336153925 | P100031 | 000 |
| 07613336153949 | P100031 | 017 |