This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
Device | P090006S001 |
Classification Name | None |
Applicant | |
PMA | P090006 |
Supplement | S001 |
Supplement Number | Date | Supplement Type |
---|---|---|
P090006 | Original Filing | |
S019 | 2016-08-17 | 135 Review Track For 30-day Notice |
S018 | 2016-07-13 | 30-day Notice |
S017 | 2016-05-05 | 30-day Notice |
S016 | 2015-09-24 | 30-day Notice |
S015 | 2015-03-20 | 135 Review Track For 30-day Notice |
S014 | 2014-03-04 | 30-day Notice |
S013 | 2014-01-09 | 30-day Notice |
S012 | 2013-12-16 | 30-day Notice |
S011 | 2013-09-16 | 30-day Notice |
S010 | 2013-04-22 | 30-day Notice |
S009 | 2013-03-11 | 135 Review Track For 30-day Notice |
S008 | 2012-03-22 | 135 Review Track For 30-day Notice |
S007 | 2011-08-08 | 30-day Notice |
S006 | 2011-04-21 | 30-day Notice |
S005 | 2011-03-01 | 30-day Notice |
S004 | 2010-12-20 | 30-day Notice |
S003 | 2010-11-26 | Normal 180 Day Track No User Fee |
S002 | 2010-07-19 | Normal 180 Day Track |
S001 |