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 | 1994-05-20 |
| Decision Date | 1994-11-28 |
| PMA | P850069 |
| Supplement | S011 |
| Product Code | LML |
| Advisory Committee | Physical Medicine |
| Supplement Type | Normal 180 Day Track |
| Supplement Reason | Location Change - Manufacturer/sterilizer/packager/supplier |
| 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 |