This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
| Device | P900007S003 |
| Classification Name | None |
| Applicant | |
| PMA | P900007 |
| Supplement | S003 |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P900007 | Original Filing | |
| S006 | 2008-12-02 | 30-day Notice |
| S005 | 2008-11-17 | Real-time Process |
| S004 | 2008-04-01 | 30-day Notice |
| S003 | ||
| S002 | 2000-01-04 | Normal 180 Day Track |
| S001 | 1998-01-15 | Normal 180 Day Track |
| Device ID | PMA | Supp |
|---|---|---|
| 00827002169081 | P900007 | 001 |
| 00827002190276 | P900007 | 002 |