This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
| Device | P010029S003 |
| Classification Name | None |
| Applicant | |
| PMA | P010029 |
| Supplement | S003 |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P010029 | Original Filing | |
| S030 | 2020-04-02 | 30-day Notice |
| S029 | 2019-12-09 | 30-day Notice |
| S028 | 2019-04-05 | 30-day Notice |
| S027 | 2018-08-22 | Real-time Process |
| S026 | 2018-03-29 | 30-day Notice |
| S025 | 2017-06-20 | Normal 180 Day Track No User Fee |
| S024 | 2015-04-23 | 30-day Notice |
| S023 | 2015-03-06 | 30-day Notice |
| S022 | 2015-02-09 | 30-day Notice |
| S021 | 2014-12-24 | 30-day Notice |
| S020 | 2014-04-28 | 30-day Notice |
| S019 | 2014-02-20 | 30-day Notice |
| S018 | 2013-11-13 | 30-day Notice |
| S017 | 2013-05-08 | 30-day Notice |
| S016 | 2013-01-15 | 30-day Notice |
| S015 | 2012-04-05 | 30-day Notice |
| S014 | 2012-03-05 | 30-day Notice |
| S013 | 2011-12-29 | 30-day Notice |
| S012 | 2011-03-02 | 30-day Notice |
| S011 | 2009-12-07 | 30-day Notice |
| S010 | 2009-11-17 | 135 Review Track For 30-day Notice |
| S009 | 2009-11-09 | 30-day Notice |
| S008 | 2009-03-30 | Panel Track |
| S007 | 2008-05-02 | 135 Review Track For 30-day Notice |
| S006 | 2007-03-22 | Real-time Process |
| S005 | ||
| S004 | 2006-09-18 | Real-time Process |
| S003 | ||
| S002 | 2005-10-05 | Normal 180 Day Track No User Fee |
| S001 | 2005-01-13 | Normal 180 Day Track |
| Device ID | PMA | Supp |
|---|---|---|
| 05060548950064 | P010029 | 000 |
| 07640128544210 | P010029 | 001 |
| 05060459970045 | P010029 | 024 |