# P990040: Trufill N-Butyl Cyanoacrylate Liquid Embolic System

- Pathway: PMA
- Applicant: Cerenovus, Inc.
- Decided: Sep 25, 2000 after 437 days
- Product code: KGG (Tissue Adhesive For Use In Embolization Of Brain Arteriovenous Malformations)
- Device class: 3
- Recalls of this device: 2 (2 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.
1 of 1 device in its family (counting itself) has 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
- Oct 11, 2013 · Class I · Z-0788-2014: Incorrect instructions for use (IFU).
- Oct 11, 2013 · Class I · Z-0789-2014: Incorrect instructions for use (IFU).

Source page: https://510kreport.com/device/P990040
Methodology: https://510kreport.com/methodology