Change to increase the syringe filling speed for restylane defyne.
Device | RESTYLANE REYNE and RESTYLANE DEFYNE INJECFTABLE GELS |
Classification Name | Implant, Dermal, For Aesthetic Use |
Generic Name | Implant, Dermal, For Aesthetic Use |
Applicant | Q-Med AB |
Date Received | 2018-05-25 |
Decision Date | 2018-06-21 |
PMA | P140029 |
Supplement | S011 |
Product Code | LMH |
Advisory Committee | General & Plastic Surgery |
Supplement Type | 30-day Notice |
Supplement Reason | Process Change - Manufacturer/sterilizer/packager/supplier |
Expedited Review | No |
Combination Product | Yes |
Applicant Address | Q-Med AB seminariegatan 21 uppsala S-752-7522 |
Supplemental Filings
Supplement Number | Date | Supplement Type |
P140029 | | Original Filing |
S047 |
2022-11-21 |
Special (immediate Track) |
S046 |
2022-09-07 |
30-day Notice |
S045 | | |
S044 |
2021-11-15 |
30-day Notice |
S043 |
2021-11-05 |
30-day Notice |
S042 |
2021-09-27 |
30-day Notice |
S041 | | |
S040 |
2021-06-02 |
135 Review Track For 30-day Notice |
S039 | | |
S038 |
2021-03-16 |
30-day Notice |
S037 |
2021-03-15 |
30-day Notice |
S036 |
2021-02-01 |
30-day Notice |
S035 | | |
S034 |
2020-10-07 |
30-day Notice |
S033 | | |
S032 | | |
S031 | | |
S030 |
2020-09-14 |
30-day Notice |
S029 | | |
S028 |
2020-07-29 |
30-day Notice |
S027 | | |
S026 |
2020-06-04 |
30-day Notice |
S025 |
2020-04-21 |
Special (immediate Track) |
S024 |
2020-02-18 |
30-day Notice |
S023 |
2020-01-21 |
30-day Notice |
S022 | | |
S021 |
2019-09-03 |
Panel Track |
S020 |
2019-08-15 |
30-day Notice |
S019 | | |
S018 | | |
S017 |
2019-05-17 |
Real-time Process |
S016 |
2019-02-14 |
30-day Notice |
S015 |
2018-10-22 |
30-day Notice |
S014 |
2018-09-19 |
30-day Notice |
S013 |
2018-08-23 |
30-day Notice |
S012 |
2018-06-01 |
30-day Notice |
S011 |
2018-05-25 |
30-day Notice |
S010 |
2018-05-23 |
30-day Notice |
S009 |
2018-05-18 |
30-day Notice |
S008 |
2018-05-16 |
30-day Notice |
S007 |
2018-04-26 |
Real-time Process |
S006 |
2017-12-18 |
135 Review Track For 30-day Notice |
S005 | | |
S004 |
2017-06-14 |
Normal 180 Day Track No User Fee |
S003 |
2017-06-08 |
30-day Notice |
S002 | | |
S001 |
2017-01-11 |
135 Review Track For 30-day Notice |
NIH GUDID Devices