This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
| Device | P060034S003 |
| Classification Name | None |
| Applicant | |
| PMA | P060034 |
| Supplement | S003 |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P060034 | Original Filing | |
| S008 | 2014-02-26 | 30-day Notice |
| S007 | 2013-11-13 | 30-day Notice |
| S006 | 2012-10-19 | 30-day Notice |
| S005 | 2010-06-17 | Normal 180 Day Track No User Fee |
| S004 | 2009-09-25 | Normal 180 Day Track |
| S003 | ||
| S002 | 2008-09-30 | Real-time Process |
| S001 | 2008-09-22 | 30-day Notice |
| Device ID | PMA | Supp |
|---|---|---|
| 00847865013178 | P060034 | 000 |
| 00847865013161 | P060034 | 000 |
| 00847865013154 | P060034 | 000 |
| 00847865013147 | P060034 | 000 |
| 00847865013130 | P060034 | 000 |
| 00847865013123 | P060034 | 000 |
| 00847865011365 | P060034 | 000 |