This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
Device | P110015S003 |
Classification Name | None |
Applicant | |
PMA | P110015 |
Supplement | S003 |
Supplement Number | Date | Supplement Type |
---|---|---|
P110015 | Original Filing | |
S010 | 2022-05-03 | 30-day Notice |
S009 | ||
S008 | 2021-03-16 | Real-time Process |
S007 | 2021-02-23 | 30-day Notice |
S006 | 2019-10-30 | 30-day Notice |
S005 | 2019-03-05 | 135 Review Track For 30-day Notice |
S004 | 2018-06-14 | 30-day Notice |
S003 | ||
S002 | 2016-07-15 | 135 Review Track For 30-day Notice |
S001 |
Device ID | PMA | Supp |
---|---|---|
M763K0211 | P110015 | 000 |