# K102169: Cyberwand Lithotripter

- Pathway: 510(k) (Special)
- Applicant: Cybersonics, Inc.
- Decided: Aug 30, 2010 after 28 days
- Product code: FFK (Lithotriptor, Electro-Hydraulic)
- Device class: 2
- Regulation: 21 CFR 876.4480
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K863642 (1986). 8 ancestors in all.
5 later devices descend from it; 2 cite it directly.
0 of 14 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K052135: Cybersonics Cyberwand Dual Probe Lithotripter, Cybersonics, Inc. (2005) Summary page 1.

## Most influential descendants
- K120303: Cyberwand Dual Action Ultrasonic Lithotripsy System (2012), 3 descendants of its own
- K142428: Shock Pulse-SE Lithotripsy System CYBERWAND II (2014), 1 descendant of its own
- K171024: ShockPulse-SE Lithotripsy System (2017), 0 descendants of its own
- K132795: Cyberwand Sterile Probe Set (2013), 0 descendants of its own
- K111058: Uretron Model Urt (2012), 0 descendants of its own

## Indications for use
The CyberWand Hollow Semi-Flexible Ureteral probe is designed to be used only with the CyberWand System for the fragmentation of urinary tract calculi in the kidneys, ureter, and bladder.

Source page: https://510kreport.com/device/K102169
Methodology: https://510kreport.com/methodology