This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
| Device | P980031S010 |
| Classification Name | None |
| Applicant | |
| PMA | P980031 |
| Supplement | S010 |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P980031 | Original Filing | |
| S012 | 2012-12-12 | 135 Review Track For 30-day Notice |
| S011 | 2012-11-14 | 30-day Notice |
| S010 | ||
| S009 | 2005-10-31 | 30-day Notice |
| S008 | 2004-06-10 | Normal 180 Day Track No User Fee |
| S007 | 2004-05-19 | Normal 180 Day Track No User Fee |
| S006 | 2003-05-14 | Normal 180 Day Track No User Fee |
| S005 | 2003-05-02 | 30-day Notice |
| S004 | 2000-02-23 | Normal 180 Day Track |
| S003 | 2000-02-22 | 30-day Notice |
| S002 | 1999-12-23 | 30-day Notice |
| S001 | 1999-11-03 | 30-day Notice |
| Device ID | PMA | Supp |
|---|---|---|
| 00866304000104 | P980031 | 000 |
| 00850048576216 | P980031 | 000 |
| 00850048576209 | P980031 | 000 |
| 00850048576193 | P980031 | 000 |