This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
Device | P180032S006 |
Classification Name | None |
Applicant | |
PMA | P180032 |
Supplement | S006 |
Supplement Number | Date | Supplement Type |
---|---|---|
P180032 | Original Filing | |
S011 | 2022-12-21 | Special (immediate Track) |
S010 | 2022-05-02 | Special (immediate Track) |
S009 | 2021-08-09 | 30-day Notice |
S008 | 2021-07-01 | 30-day Notice |
S007 | 2021-06-30 | 30-day Notice |
S006 | ||
S005 | 2021-03-29 | Special (immediate Track) |
S004 | 2021-02-01 | 30-day Notice |
S003 | 2020-10-29 | Normal 180 Day Track No User Fee |
S002 | 2020-10-21 | Special (immediate Track) |
S001 | 2020-01-03 | Normal 180 Day Track |
Device ID | PMA | Supp |
---|---|---|
00850008595035 | P180032 | 001 |
20850008595022 | P180032 | 001 |
00850008595042 | P180032 | 001 |