This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
| Device | P190024S003 |
| Classification Name | None |
| Applicant | |
| PMA | P190024 |
| Supplement | S003 |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P190024 | Original Filing | |
| S009 | 2023-01-03 | 30-day Notice |
| S008 | 2022-10-14 | 30-day Notice |
| S007 | 2022-07-12 | 30-day Notice |
| S006 | 2022-02-16 | Special (immediate Track) |
| S005 | 2022-01-28 | 135 Review Track For 30-day Notice |
| S004 | 2021-03-01 | 30-day Notice |
| S003 | ||
| S002 | 2020-08-26 | Real-time Process |
| S001 | 2020-04-28 | Normal 180 Day Track |
| Device ID | PMA | Supp |
|---|---|---|
| 04015630977215 | P190024 | 000 |