This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
| Device | P900066S012 |
| Classification Name | None |
| Applicant | |
| PMA | P900066 |
| Supplement | S012 |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P900066 | Original Filing | |
| S015 | 2022-01-06 | 30-day Notice |
| S014 | ||
| S013 | 2021-08-31 | 30-day Notice |
| S012 | ||
| S011 | 2011-12-06 | 30-day Notice |
| S010 | 2010-07-19 | 30-day Notice |
| S009 | 2009-08-13 | Special (immediate Track) |
| S008 | 2008-07-21 | 135 Review Track For 30-day Notice |
| S007 | ||
| S006 | 2002-08-13 | 135 Review Track For 30-day Notice |
| S005 | 2001-12-26 | Special (immediate Track) |
| S004 | 2000-08-18 | Special (immediate Track) |
| S003 | 1999-09-21 | Normal 180 Day Track |
| S002 | 1996-08-23 | Normal 180 Day Track |
| S001 |
| Device ID | PMA | Supp |
|---|---|---|
| 00380657971039 | P900066 | 000 |
| 00380657971022 | P900066 | 000 |
| 00380657971015 | P900066 | 000 |
| 00380657971053 | P900066 | 002 |
| 00380657971046 | P900066 | 002 |