# K133941: Mitek Arthroscopes

- Pathway: 510(k) (Traditional)
- Applicant: Medos International SARL
- Decided: Apr 18, 2014 after 116 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: 9 generations back to K921244 (1992). 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)
- K110097: Acclarent Cyclops Multi-Angle Endoscope, Acclarent, Inc. (2011) Summary page 1.
- K100577: Acclarent Cyclops Multi-Angle Endoscope, Acclarent, Inc. (2011) Summary page 1.
- K093677: Stryker Arthroscope, Stryker Endoscopy (2010) Summary page 1.
- K030096: Video Arthroscope, Models AR-3050-30, AR-3050T-30, AR-3050-70, AR-3051-30, AR-3052-30, AR3030AN, AR-3030AS, AR3030AW, Arthrex, Inc. (2003) Summary page 1.

## Indications for use
Mitek Sports Medicine Arthroscopes are indicated for use in arthroscopic procedures (such as the knee, shoulder, hip, ankle, elbow) to provide visualization during surgery.

Source page: https://510kreport.com/device/K133941
Methodology: https://510kreport.com/methodology