# K133018: Osi Q System Arthroscopes

- Pathway: 510(k) (Traditional)
- Applicant: Orthopedic Sciences, Inc.
- Decided: Feb 26, 2014 after 154 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: 1 generation back to K992782 (1999). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K091398: Arthroscope, Orthopedic Sciences, Inc. (2009) Summary page 2.
- K992782: Nuvasive Spinal Arthroscope, Models 0, 30 and 70 Degrees, Nuvasive, Inc. (1999) Summary page 2.

## Indications for use
OSI Q System Arthroscopes of appropriate size and length are indicated for use in diagnostic and operative arthroscopic procedures to provide illumination and visualization of the hip, shoulder, knee, elbow, wrist, and ankle, and also to provide illumination and visualization during open and closed arthroscopic diagnostic procedures and removal of loose bodies and soft tissue within the joint. Hip Diagnostic procedures may include: Staging of avascular necrosis Chondral injuries Joint sepsis Synovial chondomatosis Unresolved hip pain Labral tears OSI Q System Arthroscopes of appropriate size and length also are indicated for visualization and performance of arthroscopic surgical procedures on various structures of the spine, including nerve roots, foramina, intervertebral discs and the surrounding spinal structures.

Source page: https://510kreport.com/device/K133018
Methodology: https://510kreport.com/methodology