This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
| Device | P020027S031 |
| Classification Name | None |
| Applicant | |
| PMA | P020027 |
| Supplement | S031 |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P020027 | Original Filing | |
| S039 | 2021-11-18 | 30-day Notice |
| S038 | 2020-09-14 | 30-day Notice |
| S037 | ||
| S036 | 2019-06-19 | 30-day Notice |
| S035 | 2019-05-13 | 30-day Notice |
| S034 | 2018-09-28 | Real-time Process |
| S033 | 2018-06-18 | 30-day Notice |
| S032 | 2018-04-17 | 30-day Notice |
| S031 | ||
| S030 | 2017-11-20 | 30-day Notice |
| S029 | 2017-10-16 | 30-day Notice |
| S028 | 2017-09-25 | Normal 180 Day Track No User Fee |
| S027 | 2017-06-20 | 30-day Notice |
| S026 | 2017-04-26 | 30-day Notice |
| S025 | 2017-02-17 | 30-day Notice |
| S024 | 2016-08-03 | 30-day Notice |
| S023 | 2015-12-07 | Normal 180 Day Track |
| S022 | 2015-06-04 | 135 Review Track For 30-day Notice |
| S021 | 2014-08-27 | 30-day Notice |
| S020 | 2013-05-03 | 30-day Notice |
| S019 | 2012-10-31 | 30-day Notice |
| S018 | 2012-03-08 | 30-day Notice |
| S017 | 2012-02-01 | Real-time Process |
| S016 | 2011-11-22 | 30-day Notice |
| S015 | 2011-06-30 | Normal 180 Day Track |
| S014 | 2010-10-18 | Real-time Process |
| S013 | 2010-08-19 | Normal 180 Day Track |
| S012 | 2010-07-06 | Real-time Process |
| S011 | 2010-03-25 | 30-day Notice |
| S010 | 2009-05-26 | Normal 180 Day Track |
| S009 | 2008-12-02 | Normal 180 Day Track |
| S008 | 2008-03-03 | Special (immediate Track) |
| S007 | 2008-02-26 | 30-day Notice |
| S006 | 2007-08-14 | Real-time Process |
| S005 | 2006-12-06 | 30-day Notice |
| S004 | 2005-06-29 | 30-day Notice |
| S003 | 2005-04-01 | Special (immediate Track) |
| S002 | 2005-01-31 | 30-day Notice |
| S001 | 2003-09-29 | Real-time Process |
| Device ID | PMA | Supp |
|---|---|---|
| 00842768013751 | P020027 | 000 |
| 00842768013881 | P020027 | 001 |
| 00842768016677 | P020027 | 009 |