# K230966: angiOCCLUDE Ligating Clips

- Pathway: 510(k) (Traditional)
- Applicant: A2 Medical Systems, LLC
- Decided: Sep 19, 2023 after 167 days
- Product code: FZP (Clip, Implantable)
- Device class: 2
- Regulation: 21 CFR 878.4300
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K901303 (1990). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K901303: Horizon Surgical Ligating and Marking Clip, Horizon Surgical, Inc. (1990) Summary page 4.
- K982313: Horizon Titanium Clips, Horizon Tantalum Clips, Weck Closure Systems (1998) Summary page 4.

## Indications for use
angiOCCLUDE ligating clips are intended for use in procedures involving ligation of vessels or tissue structures. Surgeons should apply the appropriate size clip for the size of vessel or tissue structure to be ligated based upon their experience, judgment, and needs.

Source page: https://510kreport.com/device/K230966
Methodology: https://510kreport.com/methodology