This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
| Device | P060001S015 |
| Classification Name | None |
| Applicant | |
| PMA | P060001 |
| Supplement | S015 |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P060001 | Original Filing | |
| S035 | 2022-11-15 | 30-day Notice |
| S034 | 2022-05-25 | 30-day Notice |
| S033 | 2022-03-29 | Real-time Process |
| S032 | 2021-04-08 | 30-day Notice |
| S031 | 2020-12-10 | 30-day Notice |
| S030 | 2020-07-21 | 30-day Notice |
| S029 | 2020-05-06 | Real-time Process |
| S028 | 2019-05-24 | 30-day Notice |
| S027 | 2019-05-03 | 30-day Notice |
| S026 | 2017-11-03 | 30-day Notice |
| S025 | ||
| S024 | 2015-11-23 | 30-day Notice |
| S023 | 2015-03-16 | 30-day Notice |
| S022 | 2014-07-21 | 30-day Notice |
| S021 | 2014-06-05 | 30-day Notice |
| S020 | 2014-05-02 | Panel Track |
| S019 | 2013-01-30 | 30-day Notice |
| S018 | 2012-10-09 | 30-day Notice |
| S017 | 2012-08-21 | Normal 180 Day Track No User Fee |
| S016 | 2011-12-19 | 30-day Notice |
| S015 | ||
| S014 | 2011-05-31 | 30-day Notice |
| S013 | 2011-04-29 | 30-day Notice |
| S012 | 2011-04-27 | 30-day Notice |
| S011 | 2011-02-16 | Normal 180 Day Track No User Fee |
| S010 | 2010-09-07 | 30-day Notice |
| S009 | 2010-05-20 | 30-day Notice |
| S008 | 2010-03-29 | Special (immediate Track) |
| S007 | 2008-05-27 | 30-day Notice |
| S006 | 2008-05-16 | Normal 180 Day Track No User Fee |
| S005 | 2008-03-07 | 30-day Notice |
| S004 | 2007-12-31 | 30-day Notice |
| S003 | 2007-02-16 | Normal 180 Day Track No User Fee |
| S002 | 2007-01-31 | 135 Review Track For 30-day Notice |
| S001 | 2007-01-29 | 135 Review Track For 30-day Notice |