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3M Company

13 FDA 510(k) clearances · PMA applicant

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RecordFirmDate
KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE (P850069/S011)3M Company1994-11-28
CENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE (P850069/S010)3M Company1994-05-19
KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE (P850069/S006)3M Company1992-12-31
KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE (P850069/S009)3M Company1992-03-13
KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE (P850069/S008)3M Company1992-01-28
KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE (P850069/S007)3M Company1990-10-17
KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE (P850069/S005)3M Company1990-03-08
KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE (P850069/S004)3M Company1989-11-22
KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE (P850069/S003)3M Company1989-01-13
KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE (P850069/S002)3M Company1988-09-07
KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE (P850069/S001)3M Company1988-07-14
3M FLUOROPOLYMER CONTACT LENS (FLUROFOCON A) (P870009/S001)3M Company1988-06-21
KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE (P850069)3M Company1987-05-07

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