# K142903: neoClose 2 AutoAnchor Pack US, neoClose 4 AutoAnchor Pack US

- Pathway: 510(k) (Special)
- Applicant: Neosurgical, Ltd.
- Decided: Nov 12, 2014 after 37 days
- Product code: GCJ (Laparoscope, General & Plastic Surgery)
- Device class: 2
- Regulation: 21 CFR 876.1500
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K123280 (2013). 2 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K123280: Neoclose Hasson, Neoclose Universal, Neosurgical, Ltd. (2013) Summary page 4.
- K131688: Neoclose Hasson, Neoclose Universal, Neosurgical, Ltd. (2013) Summary page 4.

## Most influential descendants
- K173917: neoClose PDS (2018), 0 descendants of its own

## Indications for use
neoClose is intended to facilitate the delivery of absorbable AutoAnchors through soft tissues of the body during endoscopic/laparoscopic surgery.

Source page: https://510kreport.com/device/K142903
Methodology: https://510kreport.com/methodology