# K992040: Flexiscope II Arthroscopes and Accessories

- Pathway: 510(k) (Traditional)
- Applicant: Fiber Imaging Technologies, Inc.
- Decided: Aug 6, 1999 after 50 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 Schoelly Flexilux II Arthroscopes are indicated to permit a physician. or surgeon to view the operative site during an arthroscopic procedure on the knee, shoulder, jaw, wrist, ankle, and elbow.

Source page: https://510kreport.com/device/K992040
Methodology: https://510kreport.com/methodology