This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
| Device | P160050S004 |
| Classification Name | None |
| Applicant | |
| PMA | P160050 |
| Supplement | S004 |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P160050 | Original Filing | |
| S006 | 2020-04-22 | Normal 180 Day Track No User Fee |
| S005 | 2020-04-16 | Normal 180 Day Track No User Fee |
| S004 | ||
| S003 | 2019-03-19 | Real-time Process |
| S002 | 2019-03-11 | 135 Review Track For 30-day Notice |
| S001 | 2019-03-08 | Normal 180 Day Track No User Fee |
| Device ID | PMA | Supp |
|---|---|---|
| M906BARA810MM0 | P160050 | 000 |
| M906BARA88MM0 | P160050 | 000 |