# K220006: angioLOCK Polymer Ligating Clip

- Pathway: 510(k) (Traditional)
- Applicant: A2 Medical Systems, LLC
- Decided: Mar 2, 2022 after 57 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 K030311 (2003). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K030311: Hem-O-Lok XL Clip, Weck (2003) Summary page 4.

## Indications for use
angioLOCK® Non-Absorbable Polymer Ligation 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 the vessel or tissue structure to be ligated such that the clip completely encompasses the vessel or tissue structure.

Source page: https://510kreport.com/device/K220006
Methodology: https://510kreport.com/methodology