Addition of an alternate supplier for the bovine carotid artery component of the device.
Device | ARTEGRAFT COLLAGEN VASCULAR GRAFT |
Classification Name | Tissue Graft Of 6mm And Greater |
Generic Name | Tissue Graft Of 6mm And Greater |
Applicant | ARTEGRAFT, INC. |
Date Received | 2006-02-01 |
Decision Date | 2006-03-02 |
PMA | N16837 |
Supplement | S004 |
Product Code | LXA |
Advisory Committee | Cardiovascular |
Supplement Type | 30-day Notice |
Supplement Reason | Process Change - Manufacturer/sterilizer/packager/supplier |
Expedited Review | No |
Combination Product | No |
Applicant Address | ARTEGRAFT, INC. 206-208b North Center Drive north Brunswick, NJ 08902 |
Supplemental Filings
Supplement Number | Date | Supplement Type |
N16837 | | Original Filing |
S029 |
2022-12-30 |
30-day Notice |
S028 |
2022-09-16 |
30-day Notice |
S027 | | |
S026 |
2020-04-07 |
30-day Notice |
S025 |
2018-06-15 |
30-day Notice |
S024 |
2017-12-29 |
30-day Notice |
S023 |
2017-12-19 |
30-day Notice |
S022 |
2017-08-16 |
30-day Notice |
S021 |
2015-09-11 |
Real-time Process |
S020 |
2015-04-01 |
Special (immediate Track) |
S019 |
2015-03-06 |
Real-time Process |
S018 |
2014-09-04 |
30-day Notice |
S017 |
2014-07-30 |
30-day Notice |
S016 | | |
S015 |
2014-07-07 |
Special (immediate Track) |
S014 |
2014-06-11 |
Real-time Process |
S013 | | |
S012 |
2014-02-27 |
30-day Notice |
S011 |
2013-04-26 |
Normal 180 Day Track No User Fee |
S010 |
2012-09-24 |
135 Review Track For 30-day Notice |
S009 |
2011-12-28 |
135 Review Track For 30-day Notice |
S008 |
2011-09-20 |
135 Review Track For 30-day Notice |
S007 |
2009-06-22 |
30-day Notice |
S006 |
2008-08-11 |
135 Review Track For 30-day Notice |
S005 |
2006-11-03 |
Real-time Process |
S004 |
2006-02-01 |
30-day Notice |
S003 |
1999-07-29 |
Normal 180 Day Track |
S002 | | |
S001 |
1979-06-29 |
|
NIH GUDID Devices