Approval for adding an inspection for the maximum length for certain flaws where the depth cannot be accurately assessed.
| Device | TRIFECTA VALVE |
| Classification Name | Heart-valve, Non-allograft Tissue |
| Generic Name | Heart-valve, Non-allograft Tissue |
| Applicant | St. Jude Medical, Inc. |
| Date Received | 2012-07-19 |
| Decision Date | 2012-08-08 |
| PMA | P100029 |
| Supplement | S014 |
| Product Code | LWR |
| Advisory Committee | Cardiovascular |
| Supplement Type | Special (immediate Track) |
| Supplement Reason | Process Change - Manufacturer/sterilizer/packager/supplier |
| Expedited Review | No |
| Combination Product | No |
| Applicant Address | St. Jude Medical, Inc. 177 E.county Rd. B East st Paul, MN 55117 |
Supplemental Filings
| Supplement Number | Date | Supplement Type |
| P100029 | | Original Filing |
| S049 |
2022-11-18 |
30-day Notice |
| S048 |
2022-10-20 |
30-day Notice |
| S047 |
2022-10-20 |
30-day Notice |
| S046 |
2022-03-16 |
30-day Notice |
| S045 |
2021-11-08 |
30-day Notice |
| S044 | | |
| S043 |
2020-09-15 |
30-day Notice |
| S042 |
2019-11-13 |
30-day Notice |
| S041 | | |
| S040 |
2019-05-09 |
30-day Notice |
| S039 |
2019-02-27 |
30-day Notice |
| S038 |
2019-02-13 |
30-day Notice |
| S037 |
2018-10-23 |
30-day Notice |
| S036 |
2018-09-12 |
30-day Notice |
| S035 |
2018-08-13 |
Special (immediate Track) |
| S034 |
2018-05-14 |
30-day Notice |
| S033 |
2018-03-27 |
30-day Notice |
| S032 |
2018-03-22 |
30-day Notice |
| S031 |
2018-02-15 |
30-day Notice |
| S030 |
2018-02-01 |
30-day Notice |
| S029 |
2018-01-11 |
30-day Notice |
| S028 |
2017-11-28 |
30-day Notice |
| S027 |
2017-10-27 |
30-day Notice |
| S026 | | |
| S025 |
2017-03-07 |
30-day Notice |
| S024 |
2016-12-22 |
30-day Notice |
| S023 |
2016-12-09 |
30-day Notice |
| S022 |
2016-07-01 |
30-day Notice |
| S021 |
2015-10-02 |
Normal 180 Day Track |
| S020 |
2015-08-28 |
30-day Notice |
| S019 |
2015-01-21 |
30-day Notice |
| S018 |
2014-11-13 |
30-day Notice |
| S017 |
2014-09-05 |
30-day Notice |
| S016 |
2013-06-10 |
135 Review Track For 30-day Notice |
| S015 |
2013-05-28 |
135 Review Track For 30-day Notice |
| S014 |
2012-07-19 |
Special (immediate Track) |
| S013 |
2012-04-05 |
Real-time Process |
| S012 |
2012-03-27 |
30-day Notice |
| S011 |
2012-03-22 |
Special (immediate Track) |
| S010 |
2012-01-23 |
30-day Notice |
| S009 |
2011-09-27 |
30-day Notice |
| S008 |
2011-08-17 |
Real-time Process |
| S007 |
2011-08-08 |
30-day Notice |
| S006 |
2011-06-09 |
30-day Notice |
| S005 |
2011-06-06 |
30-day Notice |
| S004 |
2011-06-06 |
135 Review Track For 30-day Notice |
| S003 |
2011-05-20 |
Normal 180 Day Track No User Fee |
| S002 |
2011-04-27 |
135 Review Track For 30-day Notice |
| S001 |
2011-04-22 |
30-day Notice |
NIH GUDID Devices