This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
| Device | P000013S014 |
| Classification Name | None |
| Applicant | |
| PMA | P000013 |
| Supplement | S014 |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P000013 | Original Filing | |
| S020 | 2022-03-03 | Special (immediate Track) |
| S019 | 2022-02-03 | 30-day Notice |
| S018 | 2021-01-05 | Real-time Process |
| S017 | 2020-07-06 | Real-time Process |
| S016 | 2018-11-26 | 30-day Notice |
| S015 | 2018-09-20 | 30-day Notice |
| S014 | ||
| S013 | 2016-02-04 | 30-day Notice |
| S012 | 2015-10-01 | 30-day Notice |
| S011 | 2011-11-10 | Normal 180 Day Track No User Fee |
| S010 | 2011-10-03 | Real-time Process |
| S009 | 2009-04-16 | Special (immediate Track) |
| S008 | 2006-12-29 | Real-time Process |
| S007 | ||
| S006 | 2006-02-22 | 30-day Notice |
| S005 | 2004-09-09 | Real-time Process |
| S004 | 2004-04-15 | Real-time Process |
| S003 | 2003-08-13 | Normal 180 Day Track No User Fee |
| S002 | 2003-06-12 | Real-time Process |
| S001 | 2003-02-04 | Real-time Process |
| Device ID | PMA | Supp |
|---|---|---|
| 04546540516879 | P000013 | 001 |
| 04546540516862 | P000013 | 001 |
| 04546540516855 | P000013 | 001 |
| 04546540516848 | P000013 | 001 |
| 04546540516831 | P000013 | 001 |
| 04546540259936 | P000013 | 001 |