This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
Device | P060025S002 |
Classification Name | None |
Applicant | |
PMA | P060025 |
Supplement | S002 |
Supplement Number | Date | Supplement Type |
---|---|---|
P060025 | Original Filing | |
S014 | 2015-02-09 | Normal 180 Day Track No User Fee |
S013 | 2013-10-31 | Normal 180 Day Track No User Fee |
S012 | 2013-07-09 | Real-time Process |
S011 | 2013-03-05 | Special (immediate Track) |
S010 | 2013-02-22 | Real-time Process |
S009 | 2012-04-30 | Normal 180 Day Track No User Fee |
S008 | 2011-11-23 | 30-day Notice |
S007 | 2010-09-17 | 30-day Notice |
S006 | 2010-05-21 | Special (immediate Track) |
S005 | 2010-05-14 | Normal 180 Day Track No User Fee |
S004 | 2009-02-09 | 30-day Notice |
S003 | 2009-01-05 | Real-time Process |
S002 | ||
S001 | 2008-10-31 | 30-day Notice |
Device ID | PMA | Supp |
---|---|---|
00613994868268 | P060025 | 000 |
00613994961587 | P060025 | 000 |
00613994961594 | P060025 | 000 |
00613994961600 | P060025 | 000 |
00613994961617 | P060025 | 000 |
00613994961624 | P060025 | 000 |
00643169072503 | P060025 | 000 |
00643169072510 | P060025 | 000 |
00643169072527 | P060025 | 000 |
00643169072534 | P060025 | 000 |
00643169072541 | P060025 | 000 |
00643169072558 | P060025 | 000 |
00613994868213 | P060025 | 000 |
00613994868220 | P060025 | 000 |
00613994868237 | P060025 | 000 |
00613994868244 | P060025 | 000 |
00613994868251 | P060025 | 000 |
00613994959720 | P060025 | 000 |