This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
| Device | P160023S018 |
| Classification Name | None |
| Applicant | |
| PMA | P160023 |
| Supplement | S018 |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P160023 | Original Filing | |
| S019 | 2020-07-09 | 30-day Notice |
| S018 | ||
| S017 | 2020-02-12 | 30-day Notice |
| S016 | 2019-12-23 | Real-time Process |
| S015 | 2019-06-21 | Normal 180 Day Track |
| S014 | 2019-05-21 | 30-day Notice |
| S013 | 2019-04-19 | 30-day Notice |
| S012 | 2019-03-27 | 30-day Notice |
| S011 | 2019-03-18 | Real-time Process |
| S010 | 2019-02-21 | 30-day Notice |
| S009 | 2018-12-31 | Real-time Process |
| S008 | 2018-11-29 | 30-day Notice |
| S007 | 2018-10-03 | 30-day Notice |
| S006 | 2018-08-31 | 30-day Notice |
| S005 | 2018-07-09 | 30-day Notice |
| S004 | 2018-05-09 | 135 Review Track For 30-day Notice |
| S003 | 2018-04-20 | 30-day Notice |
| S002 | 2018-03-12 | 30-day Notice |
| S001 | 2017-08-28 | Normal 180 Day Track |
| Device ID | PMA | Supp |
|---|---|---|
| 15420045506800 | P160023 | 000 |
| 15420045506794 | P160023 | 000 |
| 15420045506787 | P160023 | 000 |