This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
| Device | P020016S009 |
| Classification Name | None |
| Applicant | |
| PMA | P020016 |
| Supplement | S009 |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P020016 | Original Filing | |
| S011 | 2019-11-18 | 30-day Notice |
| S010 | ||
| S009 | ||
| S008 | 2016-12-14 | Normal 180 Day Track No User Fee |
| S007 | 2014-11-10 | 30-day Notice |
| S006 | 2012-01-27 | 30-day Notice |
| S005 | 2010-05-18 | Normal 180 Day Track No User Fee |
| S004 | 2009-12-02 | Real-time Process |
| S003 | 2009-09-24 | Real-time Process |
| S002 | 2006-09-11 | Normal 180 Day Track No User Fee |
| S001 | 2006-04-28 | Normal 180 Day Track No User Fee |
| Device ID | PMA | Supp |
|---|---|---|
| 00841036081898 | P020016 | 006 |
| 00841036060428 | P020016 | 006 |
| 00841036060398 | P020016 | 006 |
| 00841036060343 | P020016 | 006 |
| 00841036060329 | P020016 | 006 |
| 00841036036621 | P020016 | 006 |
| 00841036036607 | P020016 | 006 |
| 00841036036584 | P020016 | 006 |
| 00841036036560 | P020016 | 006 |
| 00841036036546 | P020016 | 006 |
| 00841036036522 | P020016 | 006 |
| 00841036036508 | P020016 | 006 |
| 00841036036454 | P020016 | 006 |
| 00841036036430 | P020016 | 006 |
| 00841036011895 | P020016 | 006 |
| 00841036011871 | P020016 | 006 |
| 00841036063580 | P020016 | 006 |
| 00841036064884 | P020016 | 006 |
| 00841036081881 | P020016 | 006 |
| 00841036081874 | P020016 | 006 |
| 00841036081867 | P020016 | 006 |
| 00841036081805 | P020016 | 006 |
| 00841036081799 | P020016 | 006 |
| 00841036081782 | P020016 | 006 |
| 00841036081744 | P020016 | 006 |
| 00841036081737 | P020016 | 006 |
| 00841036081720 | P020016 | 006 |
| 00841036081713 | P020016 | 006 |
| 00841036081560 | P020016 | 006 |
| 00841036081553 | P020016 | 006 |
| 00841036081386 | P020016 | 006 |
| 00841036081348 | P020016 | 006 |
| 00841036075118 | P020016 | 006 |
| 00841036011857 | P020016 | 006 |