# P160050: Barricaid Anular Closure Device (Acd)

- Pathway: PMA
- Applicant: Intrinsic Therapeutics
- Decided: Feb 8, 2019 after 820 days
- Product code: QES (Reherniation Reduction Device)
- Device class: 3
- Recalls of this device: 1 (0 Class I)
- 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.

## Recalls of this device
- Jul 24, 2020 · Class II · Z-2798-2020: The catalog ( REF ) number on the peelable inner labels (patient sticker) that is on the inner container (box) is incorrect. It states BAR-A8-10MM instead of BAR-A8-8MM.

Source page: https://510kreport.com/device/P160050
Methodology: https://510kreport.com/methodology