This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
| Device | P130004S006 |
| Classification Name | None |
| Applicant | |
| PMA | P130004 |
| Supplement | S006 |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P130004 | Original Filing | |
| S011 | 2021-06-10 | Normal 180 Day Track No User Fee |
| S010 | 2020-12-02 | 30-day Notice |
| S009 | 2020-06-18 | 30-day Notice |
| S008 | 2019-12-11 | Normal 180 Day Track No User Fee |
| S007 | 2019-06-27 | 30-day Notice |
| S006 | ||
| S005 | 2014-09-09 | 30-day Notice |
| S004 | 2014-02-25 | 30-day Notice |
| S003 | ||
| S002 | 2014-02-07 | Normal 180 Day Track No User Fee |
| S001 | 2014-02-07 | Normal 180 Day Track No User Fee |
| Device ID | PMA | Supp |
|---|---|---|
| 00867968000011 | P130004 | 000 |
| 00867968000004 | P130004 | 000 |