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U.S. Department of Health and Human Services

Premarket Approval (PMA)

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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.
 
DeviceKENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE
Classification Nameligaments and tendons, synthetic
Generic Nameligaments and tendons, synthetic
Applicant
3M COMPANY
3m center
bldg. 275-3se-08
st. paul, MN 55144-1000
PMA NumberP850069
Supplement NumberS001
Date Received05/09/1988
Decision Date07/14/1988
Product Code
LML
Advisory Committee Physical Medicine
Supplement Typenormal 180 day track
Supplement Reason location change - manufacturer/sterilizer/packager/supplier
Expedited Review Granted? No
Combination Product No
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