This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
| Device | P080026S001 |
| Classification Name | None |
| Applicant | |
| PMA | P080026 |
| Supplement | S001 |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P080026 | Original Filing | |
| S024 | 2021-02-05 | 30-day Notice |
| S023 | 2020-11-16 | 30-day Notice |
| S022 | 2019-04-10 | 30-day Notice |
| S021 | 2017-06-27 | 135 Review Track For 30-day Notice |
| S020 | 2016-12-01 | 30-day Notice |
| S019 | 2016-11-16 | 30-day Notice |
| S018 | 2016-10-27 | 30-day Notice |
| S017 | 2016-03-28 | 30-day Notice |
| S016 | 2015-07-29 | Real-time Process |
| S015 | ||
| S014 | 2015-03-26 | 30-day Notice |
| S013 | 2014-11-10 | 30-day Notice |
| S012 | 2014-10-24 | 30-day Notice |
| S011 | 2013-11-12 | 30-day Notice |
| S010 | 2013-10-21 | 30-day Notice |
| S009 | 2013-07-23 | 30-day Notice |
| S008 | 2013-07-11 | Real-time Process |
| S007 | 2013-05-01 | 30-day Notice |
| S006 | 2013-02-15 | Normal 180 Day Track |
| S005 | 2012-12-26 | 30-day Notice |
| S004 | 2012-10-04 | 30-day Notice |
| S003 | 2012-04-02 | 135 Review Track For 30-day Notice |
| S002 | 2011-07-01 | 135 Review Track For 30-day Notice |
| S001 |
| Device ID | PMA | Supp |
|---|---|---|
| 00884999046603 | P080026 | 000 |
| 00884999042667 | P080026 | 016 |