This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
Device | P060034S003 |
Classification Name | None |
Applicant | |
PMA | P060034 |
Supplement | S003 |
Supplement Number | Date | Supplement Type |
---|---|---|
P060034 | Original Filing | |
S008 | 2014-02-26 | 30-day Notice |
S007 | 2013-11-13 | 30-day Notice |
S006 | 2012-10-19 | 30-day Notice |
S005 | 2010-06-17 | Normal 180 Day Track No User Fee |
S004 | 2009-09-25 | Normal 180 Day Track |
S003 | ||
S002 | 2008-09-30 | Real-time Process |
S001 | 2008-09-22 | 30-day Notice |
Device ID | PMA | Supp |
---|---|---|
00847865013178 | P060034 | 000 |
00847865013161 | P060034 | 000 |
00847865013154 | P060034 | 000 |
00847865013147 | P060034 | 000 |
00847865013130 | P060034 | 000 |
00847865013123 | P060034 | 000 |
00847865011365 | P060034 | 000 |