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 | KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE |
Classification Name | Ligaments And Tendons, Synthetic |
Generic Name | Ligaments And Tendons, Synthetic |
Applicant | 3M COMPANY |
Date Received | 1991-12-12 |
Decision Date | 1992-01-28 |
PMA | P850069 |
Supplement | S008 |
Product Code | LML |
Advisory Committee | Physical Medicine |
Supplement Type | Normal 180 Day Track |
Supplement Reason | Change Design/components/specifications/material |
Expedited Review | No |
Combination Product | No |
Applicant Address | 3M COMPANY 3m Center bldg. 275-3se-08 st. Paul, MN 55144-1000 |
Supplement Number | Date | Supplement Type |
---|---|---|
P850069 | Original Filing | |
S011 | 1994-05-20 | Normal 180 Day Track |
S010 | 1994-01-21 | Normal 180 Day Track |
S009 | 1991-09-13 | Normal 180 Day Track |
S008 | 1991-12-12 | Normal 180 Day Track |
S007 | 1989-08-25 | Normal 180 Day Track |
S006 | 1989-12-26 | Panel Track |
S005 | 1989-12-13 | Normal 180 Day Track |
S004 | 1989-06-02 | Normal 180 Day Track |
S003 | 1988-10-19 | Normal 180 Day Track |
S002 | 1988-08-08 | Normal 180 Day Track |
S001 | 1988-05-09 | Normal 180 Day Track |