# K252666: Articulator Arthroscopic Bur

- Pathway: 510(k) (Traditional)
- Applicant: Joint Preservation Innovations, LLC
- Decided: Nov 21, 2025 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
Longest line of descent: 8 generations back to K011083 (2001). 40 ancestors in all.
No later device cites it as a predicate yet.
0 of 41 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K071859: Stryker Crossfire System, Stryker Endoscopy (2007) Summary page 5.
- K200875: ArtiSential Laparoscopic Instruments - Electrodes, Livsmed, Inc. (2020) Summary page 5.

## Indications for use
The ArticulatorTM Arthroscopic Bur is indicated for use in orthopedic and arthroscopic procedures for the following joints: knee, shoulder, ankle, elbow, wrist, and hip, to provide abrasion, resection, debridement, and removal of bone and cartilage.

Source page: https://510kreport.com/device/K252666
Methodology: https://510kreport.com/methodology