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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
Generic NameLIGAMENTS AND TENDONS, SYNTHETIC
Applicant3M Company
3m Center
Bldg. 275-3se-08
St. Paul, MN 55144
PMA NumberP850069
Supplement NumberS005
Date Received12/13/1989
Decision Date03/08/1990
Withdrawal Date08/28/2009
Product Code LML 
Advisory Committee Orthopedic
Supplement TypeNormal 180 Day Track
Supplement Reason Location Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
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