KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE

Ligaments And Tendons, Synthetic

FDA Premarket Approval P850069

This medical device has supplements. The device description/function or indication may have changed. Be sure to look at the supplements to get an up-to-date information on device changes. The labeling included below is the version at time of approval of the original pma or panel track supplement and may not represent the most recent labeling.

Pre-market Approval Supplement Details

DeviceKENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE
Classification NameLigaments And Tendons, Synthetic
Generic NameLigaments And Tendons, Synthetic
Applicant3M COMPANY
Date Received1985-09-19
Decision Date1987-05-07
Notice Date1987-06-16
PMAP850069
SupplementS
Product CodeLML
Docket Number87M-0173
Advisory CommitteeOrthopedic
Expedited ReviewNo
Combination Product No
Applicant Address 3M COMPANY 3m Center bldg. 275-3se-08 st. Paul, MN 55144-1000

Supplemental Filings

Supplement NumberDateSupplement Type
P850069Original 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

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