This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
| Device | P120016S029 |
| Classification Name | None |
| Applicant | |
| PMA | P120016 |
| Supplement | S029 |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P120016 | Original Filing | |
| S030 | 2022-10-11 | 30-day Notice |
| S029 | ||
| S028 | 2021-02-08 | Normal 180 Day Track |
| S027 | 2019-07-08 | Normal 180 Day Track |
| S026 | 2018-11-23 | Normal 180 Day Track No User Fee |
| S025 | 2018-07-10 | Real-time Process |
| S024 | 2018-05-30 | Panel Track |
| S023 | 2017-03-20 | 30-day Notice |
| S022 | 2017-01-17 | 30-day Notice |
| S021 | 2016-11-04 | Normal 180 Day Track |
| S020 | 2016-06-03 | Real-time Process |
| S019 | 2016-01-07 | 30-day Notice |
| S018 | 2015-11-16 | 30-day Notice |
| S017 | 2015-11-03 | 135 Review Track For 30-day Notice |
| S016 | 2015-06-29 | Special (immediate Track) |
| S015 | 2015-05-18 | Real-time Process |
| S014 | 2015-04-03 | Normal 180 Day Track No User Fee |
| S013 | 2015-03-12 | 30-day Notice |
| S012 | 2015-03-03 | 30-day Notice |
| S011 | 2015-02-25 | 30-day Notice |
| S010 | 2015-02-18 | 30-day Notice |
| S009 | 2015-02-09 | 30-day Notice |
| S008 | 2014-12-12 | 30-day Notice |
| S007 | 2014-10-20 | 30-day Notice |
| S006 | 2014-09-29 | 30-day Notice |
| S005 | 2014-08-18 | 135 Review Track For 30-day Notice |
| S004 | 2014-08-18 | Real-time Process |
| S003 | 2014-06-27 | 30-day Notice |
| S002 | 2014-03-31 | Real-time Process |
| S001 | 2014-03-18 | 30-day Notice |
| Device ID | PMA | Supp |
|---|---|---|
| M729700580I1 | P120016 | 000 |
| M729700500DX1 | P120016 | 000 |
| M729800612C2 | P120016 | 024 |
| M7298001012XL2 | P120016 | 029 |