# K002764: Hydrocision Arthrojet System with Cautery and Burr

- Pathway: 510(k) (Traditional)
- Applicant: Hydrocision, Inc.
- Decided: Nov 24, 2000 after 80 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.
9 later devices descend from it; 2 cite it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K020688: Hydrocision Arthojet System with Cautery and Turboburr (2002), 8 descendants of its own
- K032529: Hydrocision Arthrojet System with Cautery, Turboburr and Curette, Models 51300, 51310 (2003), 6 descendants of its own
- K041233: Arthrojet XT (2004), 5 descendants of its own
- K122861: XTOOL (2012), 1 descendant of its own
- K213978: TELIGEN System (2022), 0 descendants of its own

Source page: https://510kreport.com/device/K002764
Methodology: https://510kreport.com/methodology