This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
Device | P130004S006 |
Classification Name | None |
Applicant | |
PMA | P130004 |
Supplement | S006 |
Supplement Number | Date | Supplement Type |
---|---|---|
P130004 | Original Filing | |
S011 | 2021-06-10 | Normal 180 Day Track No User Fee |
S010 | 2020-12-02 | 30-day Notice |
S009 | 2020-06-18 | 30-day Notice |
S008 | 2019-12-11 | Normal 180 Day Track No User Fee |
S007 | 2019-06-27 | 30-day Notice |
S006 | ||
S005 | 2014-09-09 | 30-day Notice |
S004 | 2014-02-25 | 30-day Notice |
S003 | ||
S002 | 2014-02-07 | Normal 180 Day Track No User Fee |
S001 | 2014-02-07 | Normal 180 Day Track No User Fee |
Device ID | PMA | Supp |
---|---|---|
00867968000011 | P130004 | 000 |
00867968000004 | P130004 | 000 |