This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
| Device | P040008S009 |
| Classification Name | None |
| Applicant | |
| PMA | P040008 |
| Supplement | S009 |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P040008 | Original Filing | |
| S013 | 2016-05-03 | 30-day Notice |
| S012 | 2015-07-06 | 30-day Notice |
| S011 | 2015-03-18 | 30-day Notice |
| S010 | ||
| S009 | ||
| S008 | 2014-02-03 | 30-day Notice |
| S007 | 2013-08-15 | 30-day Notice |
| S006 | 2013-02-12 | 30-day Notice |
| S005 | 2013-02-06 | 30-day Notice |
| S004 | 2012-12-18 | 30-day Notice |
| S003 | 2012-10-11 | Real-time Process |
| S002 | 2012-01-09 | 30-day Notice |
| S001 | 2008-09-04 | 30-day Notice |
| Device ID | PMA | Supp |
|---|---|---|
| 03573026156985 | P040008 | 000 |