This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
Device | P190023S005 |
Classification Name | None |
Applicant | |
PMA | P190023 |
Supplement | S005 |
Supplement Number | Date | Supplement Type |
---|---|---|
P190023 | Original Filing | |
S011 | 2022-11-18 | 30-day Notice |
S010 | 2022-08-12 | Real-time Process |
S009 | 2022-07-01 | 30-day Notice |
S008 | 2022-06-08 | 30-day Notice |
S007 | 2022-04-18 | 30-day Notice |
S006 | 2022-02-18 | 30-day Notice |
S005 | ||
S004 | 2021-11-08 | 30-day Notice |
S003 | 2021-10-25 | 135 Review Track For 30-day Notice |
S002 | ||
S001 | 2021-10-15 | Normal 180 Day Track No User Fee |