# K070724: Ios External Fixator, Model 2-0-0

- Pathway: 510(k) (Traditional)
- Applicant: Intelligent Orthopaedics, Ltd.
- Decided: May 16, 2007 after 62 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 K953406 (1995). 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)
- K031919: Ebi Xfix DFS System, Ebi, L.P. (2003) Summary page 2.

## Indications for use
The IOS fixator is intended for use in the treatment of bone conditions including fracture fixation and other bone conditions which are amenable to treatment by the use of external fixation

Source page: https://510kreport.com/device/K070724
Methodology: https://510kreport.com/methodology