Note: 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 |
Generic Name | LIGAMENTS AND TENDONS, SYNTHETIC |
Applicant | 3M COMPANY 3M CENTER BLDG. 275-3SE-08 ST. PAUL, MN 55144-1000 |
PMA Number | P850069 |
Supplement Number | S008 |
Date Received | 12/12/1991 |
Decision Date | 01/28/1992 |
Withdrawal Date
|
08/28/2009 |
Product Code |
LML |
Advisory Committee |
Orthopedic |
Supplement Type | Normal 180 Day Track |
Supplement Reason | Change Design/Components/Specifications/Material |
Expedited Review Granted? | No |
Combination Product | No |
|
|