This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
| Device | P150016S019 |
| Classification Name | None |
| Applicant | |
| PMA | P150016 |
| Supplement | S019 |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P150016 | Original Filing | |
| S022 | 2022-08-08 | 30-day Notice |
| S021 | 2021-08-16 | 30-day Notice |
| S020 | 2021-01-14 | 30-day Notice |
| S019 | ||
| S018 | 2020-05-01 | 135 Review Track For 30-day Notice |
| S017 | 2019-01-23 | 30-day Notice |
| S016 | 2018-08-17 | 30-day Notice |
| S015 | 2018-06-27 | 30-day Notice |
| S014 | 2018-05-14 | 30-day Notice |
| S013 | 2018-04-06 | 30-day Notice |
| S012 | 2018-01-22 | Real-time Process |
| S011 | 2018-01-09 | 30-day Notice |
| S010 | 2017-11-29 | Normal 180 Day Track No User Fee |
| S009 | 2017-11-28 | 135 Review Track For 30-day Notice |
| S008 | 2017-11-28 | 30-day Notice |
| S007 | 2017-11-28 | 30-day Notice |
| S006 | 2017-10-23 | 30-day Notice |
| S005 | 2017-04-10 | Real-time Process |
| S004 | ||
| S003 | 2016-10-25 | 30-day Notice |
| S002 | 2016-10-19 | 30-day Notice |
| S001 | 2016-06-29 | 30-day Notice |
| Device ID | PMA | Supp |
|---|---|---|
| 10801741099387 | P150016 | 000 |
| 10801741099363 | P150016 | 000 |
| 20801741099377 | P150016 | 000 |