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 | Monovisc High Molecular Weight Hyaluronan |
Generic Name | Acid, Hyaluronic, Intraarticular |
Applicant | Anika Therapeutics, Inc.32 Wiggins Avenuebedford, MA 01730 PMA NumberP090031 Supplement NumberS013 Date Received06/17/2022 Decision Date07/13/2022 Product Code MOZ Advisory Committee Orthopedic Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No |
Date Received | 2022-06-17 |
Decision Date | 2022-07-13 |
PMA | P090031 |
Supplement | S013 |
Product Code | MOZ |
Advisory Committee | Orthopedic |
Supplement Type | 30-day Notice |
Supplement Reason | Process Change - Manufacturer/sterilizer/packager/supplier |
Expedited Review | No |
Combination Product | No |
Applicant Address | Anika Therapeutics, Inc. 32 Wiggins Avenue bedford, MA 01730 PMA NumberP090031 Supplement NumberS013 Date Received06/17/2022 Decision Date07/13/2022 Product Code MOZ Advisory Committee Orthopedic Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No Combination ProductNo Approval Order Statement a Change In Raw Material Acceptance Testing |
Supplement Number | Date | Supplement Type |
---|---|---|
P090031 | Original Filing | |
S015 | 2022-10-12 | 30-day Notice |
S014 | 2022-10-03 | 30-day Notice |
S013 | 2022-06-17 | 30-day Notice |
S012 | 2021-09-15 | 30-day Notice |
S011 | 2021-09-15 | 30-day Notice |
S010 | 2021-08-11 | 30-day Notice |
S009 | 2019-07-19 | Normal 180 Day Track |
S008 | 2017-05-23 | Real-time Process |
S007 | 2016-08-24 | 30-day Notice |
S006 | 2016-02-10 | Special (immediate Track) |
S005 | ||
S004 | 2014-12-24 | 135 Review Track For 30-day Notice |
S003 | 2014-11-07 | Real-time Process |
S002 | 2014-06-10 | 30-day Notice |
S001 | 2014-05-08 | 30-day Notice |
Device ID | PMA | Supp |
---|---|---|
05060548950033 | P090031 | 000 |
05060459970090 | P090031 | 000 |