This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
| Device | P910061S021 |
| Classification Name | None |
| Applicant | |
| PMA | P910061 |
| Supplement | S021 |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P910061 | Original Filing | |
| S027 | 2021-12-22 | 30-day Notice |
| S026 | 2020-12-11 | 30-day Notice |
| S025 | 2019-01-04 | 30-day Notice |
| S024 | ||
| S023 | 2016-05-31 | 30-day Notice |
| S022 | 2015-10-15 | 30-day Notice |
| S021 | ||
| S020 | 2013-07-31 | 30-day Notice |
| S019 | 2009-11-02 | 30-day Notice |
| S018 | 2009-06-09 | 30-day Notice |
| S017 | 2008-06-19 | 30-day Notice |
| S016 | 2008-04-03 | 30-day Notice |
| S015 | 2006-08-30 | Real-time Process |
| S014 | 2006-04-03 | Real-time Process |
| S013 | 2006-03-30 | Real-time Process |
| S012 | 2004-03-29 | Normal 180 Day Track No User Fee |
| S011 | 2004-03-18 | Real-time Process |
| S010 | 2003-06-23 | 30-day Notice |
| S009 | 2003-06-11 | Real-time Process |
| S008 | 1999-02-10 | Real-time Process |
| S007 | 1998-12-18 | Normal 180 Day Track |
| S006 | 1998-12-01 | Real-time Process |
| S005 | 1998-10-29 | 135 Review Track For 30-day Notice |
| S004 | 1998-09-18 | Real-time Process |
| S003 | 1998-08-07 | Normal 180 Day Track |
| S002 | ||
| S001 | 1997-06-10 | Normal 180 Day Track |