# K070712: Modification to: Yelloport Port Access System

- Pathway: 510(k) (Special)
- Applicant: Surgical Innovations Group Plc
- Decided: Mar 28, 2007 after 14 days
- Product code: GCJ (Laparoscope, General & Plastic Surgery)
- Device class: 2
- Regulation: 21 CFR 876.1500
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K962193 (1996). 1 ancestor in all.
2 later devices descend 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)
- K962193: Portland Trocars, Surgical Innovations Plc (1996) Summary page 1.

## Most influential descendants
- K190592: YelloPort Elite Port Access System (2019), 1 descendant of its own
- K210495: Port Access System (2021), 0 descendants of its own

## Recalls of this device
- Jan 20, 2022 · Class II · Z-1853-2022: Laparoscopic devices have a sterile symbol included on labels but devices are non-sterile.

## Indications for use
The YelloPort port access system is indicated for use in laparoscopic procedures to give access to the abdominal cavity while maintaining pneumoperitoneum. The YelloPort port access system is also indicated for use in laparoscopic procedures to give access to the thoracic cavity.

Source page: https://510kreport.com/device/K070712
Methodology: https://510kreport.com/methodology