# K173917: neoClose PDS

- Pathway: 510(k) (Traditional)
- Applicant: Neosurgical, Ltd.
- Decided: Nov 8, 2018 after 321 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: 3 generations back to K944415 (1994). 6 ancestors in all.
No later device cites it as a predicate yet.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K081366: Kumar T-Anchors Hernia Set, Nashville Surgical Instruments (2008) Summary page 4.
- K142903: neoClose 2 AutoAnchor Pack US, neoClose 4 AutoAnchor Pack US, Neosurgical, Ltd. (2014) Summary page 4.

## Indications for use
neoClose® PDS is indicated for the approximation of soft tissue or prosthetic material during open or laparoscopic surgical procedures.

Source page: https://510kreport.com/device/K173917
Methodology: https://510kreport.com/methodology