This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
| Device | P050048S003 |
| Classification Name | None |
| Applicant | |
| PMA | P050048 |
| Supplement | S003 |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P050048 | Original Filing | |
| S009 | 2013-11-13 | 30-day Notice |
| S008 | 2012-10-19 | 30-day Notice |
| S007 | 2012-02-22 | 135 Review Track For 30-day Notice |
| S006 | 2010-06-18 | 135 Review Track For 30-day Notice |
| S005 | 2010-06-17 | Normal 180 Day Track No User Fee |
| S004 | 2009-09-28 | Normal 180 Day Track |
| S003 | ||
| S002 | 2008-09-30 | Real-time Process |
| S001 | 2008-07-01 | 30-day Notice |
| Device ID | PMA | Supp |
|---|---|---|
| 00847865002110 | P050048 | 000 |
| 00847865002103 | P050048 | 000 |
| 00847865002097 | P050048 | 000 |
| 00847865002080 | P050048 | 000 |
| 00847865002073 | P050048 | 000 |
| 00847865002066 | P050048 | 000 |
| 00847865002059 | P050048 | 000 |
| 00847865002042 | P050048 | 000 |