# K093449: Mini Lap Retractors

- Pathway: 510(k) (Special)
- Applicant: Mini Lap Technologies, Inc.
- Decided: Feb 12, 2010 after 99 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 K992904 (1999). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K070686: Mini Lap Instruments, Mini Lap Technologies, Inc. (2007) Summary page 2.

## Indications for use
The MINI LAP Instruments are a family of minimally invasive devices with the means to penetrate soft tissue to access certain areas of the human anatomy, The devices are used to manipulate other soft internal tissues.

Source page: https://510kreport.com/device/K093449
Methodology: https://510kreport.com/methodology