This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
Device | P090009S009 |
Classification Name | None |
Applicant | |
PMA | P090009 |
Supplement | S009 |
Supplement Number | Date | Supplement Type |
---|---|---|
P090009 | Original Filing | |
S018 | 2018-10-26 | Normal 180 Day Track No User Fee |
S017 | 2017-10-11 | Real-time Process |
S016 | 2017-08-03 | 30-day Notice |
S015 | 2016-02-16 | 30-day Notice |
S014 | 2016-01-27 | 30-day Notice |
S013 | 2015-10-07 | 30-day Notice |
S012 | 2014-08-22 | 30-day Notice |
S011 | 2012-11-30 | 30-day Notice |
S010 | 2012-09-05 | 30-day Notice |
S009 | ||
S008 | 2012-02-29 | 30-day Notice |
S007 | 2012-01-31 | 135 Review Track For 30-day Notice |
S006 | 2011-11-21 | 30-day Notice |
S005 | 2011-08-29 | 135 Review Track For 30-day Notice |
S004 | 2011-08-17 | 135 Review Track For 30-day Notice |
S003 | 2011-05-17 | Normal 180 Day Track No User Fee |
S002 | 2011-04-11 | 30-day Notice |
S001 | 2010-07-28 | Normal 180 Day Track |