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.
Device | PRO-Kinetic Energy Coronary Stent System |
Generic Name | Stent, Coronary |
Applicant | BIOTRONIK, INC.6024 Jean Roadlake Oswego, OR 97035 PMA NumberP160003 Supplement NumberS015 Date Received06/21/2022 Decision Date07/27/2022 Product Code MAF Advisory Committee Cardiovascular Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No |
Date Received | 2022-06-21 |
Decision Date | 2022-07-27 |
PMA | P160003 |
Supplement | S015 |
Product Code | MAF |
Advisory Committee | Cardiovascular |
Supplement Type | 30-day Notice |
Supplement Reason | Process Change - Manufacturer/sterilizer/packager/supplier |
Expedited Review | No |
Combination Product | No |
Applicant Address | BIOTRONIK, INC. 6024 Jean Road lake Oswego, OR 97035 PMA NumberP160003 Supplement NumberS015 Date Received06/21/2022 Decision Date07/27/2022 Product Code MAF Advisory Committee Cardiovascular Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No Combination ProductNo Approval Order Statement addition Of Alternative Packaging Verification Testing |
Supplement Number | Date | Supplement Type |
---|---|---|
P160003 | Original Filing | |
S015 | 2022-06-21 | 30-day Notice |
S014 | 2021-06-14 | 30-day Notice |
S013 | 2021-04-08 | 30-day Notice |
S012 | 2021-03-25 | 30-day Notice |
S011 | ||
S010 | 2020-07-09 | 30-day Notice |
S009 | 2019-11-04 | 30-day Notice |
S008 | 2019-05-06 | 30-day Notice |
S007 | ||
S006 | 2018-06-29 | 135 Review Track For 30-day Notice |
S005 | 2018-05-10 | Normal 180 Day Track No User Fee |
S004 | 2018-04-16 | 30-day Notice |
S003 | ||
S002 | 2017-04-19 | 135 Review Track For 30-day Notice |
S001 | 2017-02-22 | 30-day Notice |