This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
| Device | P050046S008 |
| Classification Name | None |
| Applicant | |
| PMA | P050046 |
| Supplement | S008 |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P050046 | Original Filing | |
| S032 | 2021-09-01 | 30-day Notice |
| S031 | 2021-03-08 | 30-day Notice |
| S030 | 2021-01-11 | 30-day Notice |
| S029 | 2018-07-13 | 30-day Notice |
| S028 | 2018-03-26 | 30-day Notice |
| S027 | ||
| S026 | 2015-06-22 | 30-day Notice |
| S025 | 2015-06-05 | 30-day Notice |
| S024 | 2014-07-25 | 30-day Notice |
| S023 | 2014-01-28 | Real-time Process |
| S022 | 2013-11-18 | 30-day Notice |
| S021 | 2013-08-29 | 30-day Notice |
| S020 | 2013-08-19 | 30-day Notice |
| S019 | 2012-11-14 | Real-time Process |
| S018 | 2012-11-08 | 30-day Notice |
| S017 | 2012-10-02 | 30-day Notice |
| S016 | 2012-09-04 | 30-day Notice |
| S015 | 2012-07-30 | 30-day Notice |
| S014 | 2012-03-26 | 30-day Notice |
| S013 | 2012-01-24 | 30-day Notice |
| S012 | 2011-12-02 | Real-time Process |
| S011 | 2011-05-25 | 30-day Notice |
| S010 | 2011-04-01 | 30-day Notice |
| S009 | 2011-01-26 | 135 Review Track For 30-day Notice |
| S008 | ||
| S007 | 2010-08-23 | 30-day Notice |
| S006 | 2009-12-18 | 30-day Notice |
| S005 | 2009-12-16 | 30-day Notice |
| S004 | 2009-02-04 | 135 Review Track For 30-day Notice |
| S003 | 2008-08-01 | 30-day Notice |
| S002 | 2007-11-23 | Real-time Process |
| S001 |
| Device ID | PMA | Supp |
|---|---|---|
| 00802526419447 | P050046 | 000 |
| 00802526419324 | P050046 | 000 |