This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
| Device | P180032S006 |
| Classification Name | None |
| Applicant | |
| PMA | P180032 |
| Supplement | S006 |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P180032 | Original Filing | |
| S011 | 2022-12-21 | Special (immediate Track) |
| S010 | 2022-05-02 | Special (immediate Track) |
| S009 | 2021-08-09 | 30-day Notice |
| S008 | 2021-07-01 | 30-day Notice |
| S007 | 2021-06-30 | 30-day Notice |
| S006 | ||
| S005 | 2021-03-29 | Special (immediate Track) |
| S004 | 2021-02-01 | 30-day Notice |
| S003 | 2020-10-29 | Normal 180 Day Track No User Fee |
| S002 | 2020-10-21 | Special (immediate Track) |
| S001 | 2020-01-03 | Normal 180 Day Track |
| Device ID | PMA | Supp |
|---|---|---|
| 00850008595035 | P180032 | 001 |
| 20850008595022 | P180032 | 001 |
| 00850008595042 | P180032 | 001 |