# K131375: Autolap System

- Pathway: 510(k) (Traditional)
- Applicant: Mst - Medical Surgery Technologies, Ltd.
- Decided: Sep 19, 2013 after 129 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: 5 generations back to K931783 (1993). 5 ancestors in all.
3 later devices descend from it; 1 cites it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K062968: Lapman Laparoscope Manipulator and Accessories, Model 900-200 Series, Medsys, S.A. (2007) Summary page 1.

## Most influential descendants
- K152848: Autolap System (2015), 2 descendants of its own
- K242323: Maestro System (REF100) (2025), 1 descendant of its own
- K250984: Maestro System (REF100) (2025), 0 descendants of its own

## Indications for use
The AutoLap System is indicated for General laparoscopic, Gynecologic and Urologic procedures for the purpose of holding and controlling the movement of a standard laparoscope or rigid endoscope within surgical cavities during minimally invasive laparoscopic surgery.

Source page: https://510kreport.com/device/K131375
Methodology: https://510kreport.com/methodology