# K973005: The Corifix Ligament Anchor

- Pathway: 510(k) (Traditional)
- Applicant: Corin USA
- Decided: Nov 10, 1997 after 89 days
- Product code: HWC (Screw, Fixation, Bone)
- Device class: 2
- Regulation: 21 CFR 888.3040
- 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. The FDA summary names its predicate without a number.
- (no number) (Linvatec) Concept 6.3mimn Screw and Spiked Washer Anchoring Implant: named in the summary without a submission number

## Indications for use
For use 1n conjunction with the patient’s medial hamstring tendons, namely semitendinosus and gracilis, by securing the looped tendons to the femur and tibia in order to repair damnaged anterior and posterior cruciatc ligaments. Relief of pain and restoration of kuce function arising from damage to anterior ot postenor cruciate ligaments,

Source page: https://510kreport.com/device/K973005
Methodology: https://510kreport.com/methodology