This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
| Device | P050034S018 |
| Classification Name | None |
| Applicant | |
| PMA | P050034 |
| Supplement | S018 |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P050034 | Original Filing | |
| S020 | 2018-09-11 | Normal 180 Day Track No User Fee |
| S019 | 2017-09-21 | 30-day Notice |
| S018 | ||
| S017 | 2016-09-26 | 30-day Notice |
| S016 | 2016-09-23 | Real-time Process |
| S015 | 2014-11-28 | Normal 180 Day Track No User Fee |
| S014 | 2014-06-11 | Real-time Process |
| S013 | 2013-12-26 | Normal 180 Day Track |
| S012 | 2013-12-12 | 30-day Notice |
| S011 | 2013-08-08 | 30-day Notice |
| S010 | 2013-07-16 | 30-day Notice |
| S009 | 2013-05-15 | Normal 180 Day Track No User Fee |
| S008 | 2012-12-20 | 30-day Notice |
| S007 | 2012-12-04 | 30-day Notice |
| S006 | 2011-12-27 | Real-time Process |
| S005 | 2011-03-02 | 30-day Notice |
| S004 | 2010-12-15 | Real-time Process |
| S003 | 2010-09-29 | 30-day Notice |
| S002 | 2010-08-30 | Normal 180 Day Track No User Fee |
| S001 | 2010-08-30 | Normal 180 Day Track No User Fee |
| Device ID | PMA | Supp |
|---|---|---|
| M687PR00020000 | P050034 | 012 |
| M687PR00018000 | P050034 | 012 |