# K143220: SIDEKICK EZ FRAME External Fixation System

- Pathway: 510(k) (Traditional)
- Applicant: Wrightmedicaltechnologyinc
- Decided: Jan 8, 2015 after 59 days
- Product code: KTT (Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component)
- Device class: 2
- Regulation: 21 CFR 888.3030
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K043289 (2005). 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)
- K130044: Sidekick EZ Frame External Fixation System, Wrightmedicaltechnologyinc (2013) Summary page 4.

## Indications for use
Wright’s SIDEKICK® EZ FRAME™ External Fixation System is intended for: • Triple Arthrodesis • Isolated Rearfoot Arthrodesis • Midfoot Arthrodesis • Comminuted Trauma • Diabetic Charcot Reconstruction • Most foot pathology not requiring fixation above the ankle

Source page: https://510kreport.com/device/K143220
Methodology: https://510kreport.com/methodology