This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
| Device | P990040S018 |
| Classification Name | None |
| Applicant | |
| PMA | P990040 |
| Supplement | S018 |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P990040 | Original Filing | |
| S029 | 2019-02-19 | Normal 180 Day Track |
| S028 | 2018-11-15 | 30-day Notice |
| S027 | 2018-11-02 | Normal 180 Day Track No User Fee |
| S026 | 2018-05-29 | 30-day Notice |
| S025 | 2017-06-08 | 30-day Notice |
| S024 | 2017-01-31 | Normal 180 Day Track |
| S023 | 2016-11-14 | 30-day Notice |
| S022 | 2016-04-18 | Normal 180 Day Track |
| S021 | 2015-08-28 | 30-day Notice |
| S020 | 2015-02-18 | Real-time Process |
| S019 | 2014-09-17 | Real-time Process |
| S018 | ||
| S017 | 2013-09-16 | 135 Review Track For 30-day Notice |
| S016 | 2010-11-24 | 30-day Notice |
| S015 | 2010-11-08 | Real-time Process |
| S014 | 2010-10-12 | 30-day Notice |
| S013 | 2010-08-18 | 135 Review Track For 30-day Notice |
| S012 | 2010-07-28 | Real-time Process |
| S011 | 2010-05-10 | 30-day Notice |
| S010 | 2009-11-13 | 30-day Notice |
| S009 | 2009-08-31 | Normal 180 Day Track No User Fee |
| S008 | 2009-03-13 | 30-day Notice |
| S007 | 2008-12-19 | 30-day Notice |
| S006 | 2007-11-01 | 30-day Notice |
| S005 | 2007-07-20 | 135 Review Track For 30-day Notice |
| S004 | 2006-04-28 | Special (immediate Track) |
| S003 | 2006-02-09 | 30-day Notice |
| S002 | 2006-02-09 | 30-day Notice |
| S001 | 2001-03-01 | Normal 180 Day Track |
| Device ID | PMA | Supp |
|---|---|---|
| 10886704029151 | P990040 | 001 |
| 10886704029144 | P990040 | 001 |
| 10886704085324 | P990040 | 031 |
| 10886704085317 | P990040 | 031 |