# K170331: Cyber Ho

- Pathway: 510(k) (Special)
- Applicant: Quanta System Spa
- Decided: Mar 3, 2017 after 29 days
- Product code: GEX (Powered Laser Surgical Instrument)
- Device class: 2
- Regulation: 21 CFR 878.4810
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 8 generations back to K936109 (1994). 35 ancestors in all.
9 later devices descend from it; 1 cites it directly.
0 of 45 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K163009: Litho, Quanta System Spa (2016) Summary page 5.
- K140388: Lumenis Pulse 120H, Lumenis, Ltd. (2014) Summary page 5.

## Most influential descendants
- K172025: Litho 60 (2017), 8 descendants of its own
- K180922: Empower H100, Cyber Ho 100, Litho 100 (2018), 6 descendants of its own
- K192600: Cyber Ho 60, Cyber Ho 100, Litho 100, Litho 60 (2020), 5 descendants of its own
- K201455: Litho 150, Cyber Ho 150 (2020), 3 descendants of its own
- K180423: Empower H65 (2018), 1 descendant of its own

## Indications for use
The Cyber Ho laser system, including a fiber optic delivery system, is indicated for use in surgical procedures such as open, laparoscopic and endoscopic, to perform incision, excision, resection, ablation, vaporization, coagulation and hemostasis of soft tissue and in Lithotripsy of stones. It is indicated in medical specialties including, but not limited to: * Urology * Gastroenterology * Arthroscopy * Neurosurgery * Pulmonary * Gynecology * ENT * Dermatology * Plastic Surgery * General Surgery

Source page: https://510kreport.com/device/K170331
Methodology: https://510kreport.com/methodology