# K982266: Hydrocision Arthrojet System

- Pathway: 510(k) (Traditional)
- Applicant: Hydrocision, Inc.
- Decided: Sep 25, 1998 after 88 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
No predicates in its family tree.
34 later devices descend from it; 4 cite it directly.
0 of 35 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Dyonics Articular Shaver System: named in the summary without a submission number

## Most influential descendants
- K991383: Hydrocision Debdridement System (2000), 31 descendants of its own
- K012464: Helix Hydro-Jet (2001), 19 descendants of its own
- K022613: Helix Hydro-Jet (2002), 17 descendants of its own
- K033590: Erbe Helix Hydro-Jet (2004), 16 descendants of its own
- K072404: Erbe Erbejet 2 System (2007), 14 descendants of its own

## Indications for use
The ArthroJet system is intended to resect damaged tissue and remove extraneous matter found in articular body cavities. The system may be used open or arthroscopically to resect tears and other defects, remove loose fragments, shave away debris and perform appropriate synovectomy procedures.

Source page: https://510kreport.com/device/K982266
Methodology: https://510kreport.com/methodology