This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
| Device | P040025S003 |
| Classification Name | None |
| Applicant | |
| PMA | P040025 |
| Supplement | S003 |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P040025 | Original Filing | |
| S014 | 2013-06-26 | Normal 180 Day Track No User Fee |
| S013 | 2013-05-28 | Normal 180 Day Track |
| S012 | 2012-01-26 | Real-time Process |
| S011 | 2010-09-29 | Real-time Process |
| S010 | 2010-05-03 | Real-time Process |
| S009 | 2009-07-21 | Real-time Process |
| S008 | 2008-10-27 | Real-time Process |
| S007 | 2008-07-16 | Normal 180 Day Track |
| S006 | 2007-10-24 | Real-time Process |
| S005 | 2007-08-24 | 30-day Notice |
| S004 | ||
| S003 | ||
| S002 | ||
| S001 |
| Device ID | PMA | Supp |
|---|---|---|
| 00382830016308 | P040025 | 000 |
| 00382830009584 | P040025 | 000 |
| 00382830009577 | P040025 | 000 |
| 00382830009560 | P040025 | 000 |
| 00382830004169 | P040025 | 000 |