This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
| Device | P180007S001 |
| Classification Name | None |
| Applicant | |
| PMA | P180007 |
| Supplement | S001 |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P180007 | Original Filing | |
| S009 | 2022-04-12 | 30-day Notice |
| S008 | 2021-04-30 | Normal 180 Day Track No User Fee |
| S007 | 2020-10-21 | Normal 180 Day Track No User Fee |
| S006 | ||
| S005 | 2019-11-18 | Normal 180 Day Track |
| S004 | ||
| S003 | 2018-12-26 | Normal 180 Day Track No User Fee |
| S002 | 2018-12-26 | Normal 180 Day Track No User Fee |
| S001 |
| Device ID | PMA | Supp |
|---|---|---|
| 00896506002323 | P180007 | 000 |
| 00896506002316 | P180007 | 000 |
| 00896506002309 | P180007 | 000 |
| 00896506002293 | P180007 | 000 |
| 00896506002286 | P180007 | 000 |
| 00896506002279 | P180007 | 000 |