# K992621: Adi 9000/9001 Arthroscope and Accessories

- Pathway: 510(k) (Traditional)
- Applicant: Advanced Diagnostics & Interventions
- Decided: Nov 8, 1999 after 95 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.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The arthroscope and accessories are intended to be used by a licensed physician, for the purpose of joint arthroscopic procedures.

Source page: https://510kreport.com/device/K992621
Methodology: https://510kreport.com/methodology