This medical device record is a pma supplement. A supplement may have changed the device description/function or indication from that approved in the original pma. Be sure to look at the original pma record for more information.
Increase in sterilization cycle capacity.
Device | RELAY THORACIC STENT-GRAFT WITH PLUS DELIVERY SYSTEM |
Classification Name | System, Endovascular Graft, Aortic Aneurysm Treatment |
Generic Name | System, Endovascular Graft, Aortic Aneurysm Treatment |
Applicant | BOLTON MEDICAL, INC. |
Date Received | 2014-03-24 |
Decision Date | 2014-04-16 |
PMA | P110038 |
Supplement | S004 |
Product Code | MIH |
Advisory Committee | Cardiovascular |
Supplement Type | 30-day Notice |
Supplement Reason | Process Change - Manufacturer/sterilizer/packager/supplier |
Expedited Review | No |
Combination Product | No |
Applicant Address | BOLTON MEDICAL, INC. 799 International Parkway sunrise, FL 33325 |
Supplement Number | Date | Supplement Type |
---|---|---|
P110038 | Original Filing | |
S027 | 2022-12-23 | Special (immediate Track) |
S026 | 2022-07-12 | 30-day Notice |
S025 | 2020-11-24 | 30-day Notice |
S024 | 2019-09-30 | 30-day Notice |
S023 | 2019-03-20 | 30-day Notice |
S022 | ||
S021 | ||
S020 | 2018-10-05 | 30-day Notice |
S019 | ||
S018 | 2018-05-17 | Special (immediate Track) |
S017 | 2017-12-07 | Normal 180 Day Track No User Fee |
S016 | 2017-11-17 | Special (immediate Track) |
S015 | 2017-04-07 | 30-day Notice |
S014 | 2016-09-16 | 30-day Notice |
S013 | 2016-08-29 | 135 Review Track For 30-day Notice |
S012 | 2016-06-21 | Real-time Process |
S011 | 2016-02-22 | Real-time Process |
S010 | 2015-10-19 | Special (immediate Track) |
S009 | 2015-01-06 | Normal 180 Day Track No User Fee |
S008 | 2014-11-14 | 30-day Notice |
S007 | ||
S006 | 2014-09-15 | 30-day Notice |
S005 | 2014-05-12 | 30-day Notice |
S004 | 2014-03-24 | 30-day Notice |
S003 | ||
S002 | 2013-06-10 | 30-day Notice |
S001 | 2012-10-19 | Normal 180 Day Track No User Fee |