This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
| Device | P890017S001 |
| Classification Name | None |
| Applicant | |
| PMA | P890017 |
| Supplement | S001 |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P890017 | Original Filing | |
| S023 | 2022-09-28 | Real-time Process |
| S022 | 2021-12-08 | Real-time Process |
| S021 | ||
| S020 | 2019-07-23 | 30-day Notice |
| S019 | 2016-11-01 | 30-day Notice |
| S018 | 2016-03-01 | 135 Review Track For 30-day Notice |
| S017 | 2015-06-24 | 135 Review Track For 30-day Notice |
| S016 | 2015-03-17 | 30-day Notice |
| S015 | 2009-10-01 | 30-day Notice |
| S014 | 2006-01-20 | Real-time Process |
| S013 | ||
| S012 | ||
| S011 | 2003-04-15 | Normal 180 Day Track |
| S010 | 2001-12-06 | Panel Track |
| S009 | 2000-05-26 | Special (immediate Track) |
| S008 | 2000-03-23 | Normal 180 Day Track |
| S007 | 1999-07-16 | Normal 180 Day Track |
| S006 | 1998-12-31 | Normal 180 Day Track |
| S005 | 1998-09-02 | 30-day Notice |
| S004 | 1994-02-22 | Normal 180 Day Track |
| S003 | ||
| S002 | 1992-04-06 | Normal 180 Day Track |
| S001 |
| Device ID | PMA | Supp |
|---|---|---|
| 20705032057292 | P890017 | 015 |
| 20705032057346 | P890017 | 015 |
| 20705032057247 | P890017 | 015 |
| 20705032057223 | P890017 | 015 |
| 20705032057261 | P890017 | 015 |
| 20705032057285 | P890017 | 015 |
| 20705032057315 | P890017 | 015 |