This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
Device | P010055S008 |
Classification Name | None |
Applicant | |
PMA | P010055 |
Supplement | S008 |
Supplement Number | Date | Supplement Type |
---|---|---|
P010055 | Original Filing | |
S011 | 2021-06-03 | 30-day Notice |
S010 | ||
S009 | 2014-02-21 | Normal 180 Day Track No User Fee |
S008 | ||
S007 | 2009-09-09 | Normal 180 Day Track |
S006 | 2009-04-02 | Normal 180 Day Track No User Fee |
S005 | 2009-04-02 | Normal 180 Day Track No User Fee |
S004 | 2007-05-25 | 30-day Notice |
S003 | 2006-11-22 | 30-day Notice |
S002 | 2004-09-30 | Normal 180 Day Track No User Fee |
S001 | 2004-07-30 | Normal 180 Day Track |
Device ID | PMA | Supp |
---|---|---|
07350081910082 | P010055 | 009 |
07350081910075 | P010055 | 009 |
07350081910068 | P010055 | 009 |
07350081910051 | P010055 | 009 |
07350081910044 | P010055 | 009 |
07350081910037 | P010055 | 009 |
07350081910020 | P010055 | 009 |
07350081910013 | P010055 | 009 |