# K111412: Surgisteer Scissors, Surgisteer Dissector / Grasper, Surgisteer Hook

- Pathway: 510(k) (Traditional)
- Applicant: Steerable Technologix
- Decided: Sep 30, 2011 after 133 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: 3 generations back to K910831 (1991). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K061425: Purewrist Scissors, Model PW1101-01;Purewrist Dissector,  Model PW1201-01;Purewrist Hook, Model PW1301-01, Cambridge Endoscopic Devices (2006) Summary page 1.

## Indications for use
The SurgisteerM line of of electrocautery laparoscopic instruments are sterile, single-use devices intended for use in a variety of minimally invasive surgical procedures to facilitate grasping, mobilization, dissection, and transection of tissue.

Source page: https://510kreport.com/device/K111412
Methodology: https://510kreport.com/methodology