# P220024: LIQUIFIX FIX8 Hernia Mesh Fixation (HMF) Device, LIQUIFIX Precision Open Hernia Mesh Fixation Device

- Pathway: PMA
- Applicant: Advanced Medical Solutions Limited
- Decided: Jun 2, 2023 after 218 days
- Product code: PLJ (Tissue Adhesive Internal Use)
- Device class: 3
- Regulation: 21 CFR 878.4010
- 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/P220024
Methodology: https://510kreport.com/methodology