# K063485: Logic Laparoscopic Scissors

- Pathway: 510(k) (Traditional)
- Applicant: Surgical Innovations Plc
- Decided: Dec 1, 2006 after 14 days
- Product code: GEI (Electrosurgical, Cutting & Coagulation & Accessories)
- Device class: 2
- Regulation: 21 CFR 878.4400
- 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 K932648 (1993). 11 ancestors in all.
7 later devices descend from it; 2 cite it directly.
0 of 19 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K040295: Applied Laparoscopic Monopolar Scissors, Applied Medical Resources Corp. (2004) Summary page 1.
- K014207: Reposable Instrument System, Models MF001-MF083, Aesculap, Inc. (2002) Summary page 1.

## Most influential descendants
- K090583: Endoscopic Monopolar Scissors, Models Ems-235, Ems-165 (2009), 4 descendants of its own
- K141058: Ensizor Endoscopic Scissors (2014), 3 descendants of its own
- K150939: Ensizor Endoscopic Scissors (2015), 2 descendants of its own
- K100109: Logiflex Laparoscopic Band Positioning Device (2010), 1 descendant of its own
- K242923: SimpleSnip Endoscopic Suture Cutter (SC500160); SimpleSnip Endoscopic Suture Cutter (SC500230) (2024), 0 descendants of its own

## Indications for use
Surgical Innovations Resposable Laparoscopic Scissors are designed to cut, dissect, manipulate and/or cauterize various tissue during endoscopic/laparoscopic, general, vascular gynaecological and thoracic surgical procedures.

Source page: https://510kreport.com/device/K063485
Methodology: https://510kreport.com/methodology