# P850069: Kennedy Lad (TM) Ligament Augmentation Device

- Pathway: PMA
- Applicant: 3M Company
- Decided: May 7, 1987 after 595 days
- Product code: LML (Ligaments And Tendons, Synthetic)
- Device class: 3
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. PMA decisions do not claim a predicate device.

Source page: https://510kreport.com/device/P850069
Methodology: https://510kreport.com/methodology