# K023783: Sohniks

- Pathway: 510(k) (Traditional)
- Applicant: Sohniks Endoscopy, Inc.
- Decided: Feb 7, 2003 after 87 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.
1 later device descends from it; 1 cites it directly.
0 of 2 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 no predicate by number.

## Most influential descendants
- K033191: Sohniks (2004), 0 descendants of its own

## Indications for use
The Soliniks Endoscopy Arthroscopes are intended for use by qualified surgeons during procedures of sinall and large joints. The intended use for Sirhniks Endoscopy, Inc.’s arthroscopes are for examining, diagnosing, visualizing and to aid in treating the interior probleiiis of orthopedic joints, otolaryngology,rhinology, endoscopic plastic and rcwnstructive surgery. Our arthroscopes are intended for use in the shoulder, wrist, knee:, ankle, elbow, and jaw and visualimtion of the hip joint to diagnose disease and removal of loose bodies.

Source page: https://510kreport.com/device/K023783
Methodology: https://510kreport.com/methodology