# K123280: Neoclose Hasson, Neoclose Universal

- Pathway: 510(k) (Traditional)
- Applicant: Neosurgical, Ltd.
- Decided: Apr 18, 2013 after 178 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
No predicates in its family tree.
5 later devices descend from it; 3 cite it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Carter-Thomason CloseSure System®: named in the summary without a submission number

## Most influential descendants
- K131688: Neoclose Hasson, Neoclose Universal (2013), 2 descendants of its own
- K160564: TroClose1200 (2016), 1 descendant of its own
- K142903: neoClose 2 AutoAnchor Pack US, neoClose 4 AutoAnchor Pack US (2014), 1 descendant of its own
- K253620: TroClose 1200 (2025), 0 descendants of its own
- K173917: neoClose PDS (2018), 0 descendants of its own

## Indications for use
The neoClose device 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/K123280
Methodology: https://510kreport.com/methodology