This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
| Device | P030023S003 |
| Classification Name | None |
| Applicant | |
| PMA | P030023 |
| Supplement | S003 |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P030023 | Original Filing | |
| S008 | 2022-02-08 | 30-day Notice |
| S007 | 2018-12-18 | 30-day Notice |
| S006 | ||
| S005 | 2016-06-10 | 30-day Notice |
| S004 | 2014-07-21 | Normal 180 Day Track |
| S003 | ||
| S002 | 2012-01-05 | 135 Review Track For 30-day Notice |
| S001 | 2011-10-19 | Normal 180 Day Track No User Fee |
| Device ID | PMA | Supp |
|---|---|---|
| 08717819070286 | P030023 | 004 |
| 08717819070279 | P030023 | 004 |