# K200729: HydroCision SpineJet System

- Pathway: 510(k) (Special)
- Applicant: Hydrocision, Inc.
- Decided: Apr 16, 2020 after 27 days
- Product code: HRX (Arthroscope)
- Device class: 2
- Regulation: 21 CFR 888.1100
- 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 K002764 (2000). 5 ancestors in all.
No later device cites it as a predicate yet.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K041233: Arthrojet XT, Hydrocision, Inc. (2004) Summary page 5.

## Indications for use
The HydroCision SpineJet System is indicated for surgical procedures where the cutting and removal of soft tissue and the ablation and removal of hard tissue or bone is required. Specific functions include cutting, ablation and shaping of soft tissue, and decorticating and smoothing of bone, cartilage and other bone related tissue in open and minimally invasive spinal surgeries.

Source page: https://510kreport.com/device/K200729
Methodology: https://510kreport.com/methodology