This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
Device | P170018S005 |
Classification Name | None |
Applicant | |
PMA | P170018 |
Supplement | S005 |
Supplement Number | Date | Supplement Type |
---|---|---|
P170018 | Original Filing | |
S015 | 2022-10-13 | Real-time Process |
S014 | 2022-07-27 | Real-time Process |
S013 | 2021-05-17 | 30-day Notice |
S012 | 2021-01-25 | Special (immediate Track) |
S011 | 2020-10-02 | 30-day Notice |
S010 | 2020-09-11 | 30-day Notice |
S009 | 2020-09-10 | 30-day Notice |
S008 | 2020-08-26 | 30-day Notice |
S007 | 2020-06-12 | Real-time Process |
S006 | 2020-04-23 | 30-day Notice |
S005 | ||
S004 | 2019-09-11 | Real-time Process |
S003 | 2019-01-15 | Real-time Process |
S002 | 2019-01-11 | Real-time Process |
S001 | 2018-12-31 | 30-day Notice |
Device ID | PMA | Supp |
---|---|---|
00883873867808 | P170018 | 000 |
00883873871577 | P170018 | 000 |
00883873790687 | P170018 | 000 |
00883873824061 | P170018 | 002 |
00883873824078 | P170018 | 002 |
00883873824085 | P170018 | 002 |
00883873824092 | P170018 | 002 |
00883873824108 | P170018 | 002 |
00883873824115 | P170018 | 002 |
00883873824122 | P170018 | 002 |
00883873824139 | P170018 | 002 |