# K052239: Ebi Dynafix Vision Footplate System

- Pathway: 510(k) (Traditional)
- Applicant: Ebi, L.P.
- Decided: Sep 21, 2005 after 35 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
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 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 its predicate without a number.
- (no number) EBI XFIX DFS System: named in the summary without a submission number
- (no number) EBI XFIX Vision Fixation System: named in the summary without a submission number
- (no number) Howmedica Osteonics Corporation Hoffmann II Foot Ring: named in the summary without a submission number

## Most influential descendants
- K071395: Biomet Vision Footring System (2007), 1 descendant of its own
- K093753: Mdpo Frame System (2010), 0 descendants of its own

## Indications for use
The EBI® DynaFix® Vision® FootPlate System intended for use in the treatment of bone conditions including osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by the use of the external fixation modality.

Source page: https://510kreport.com/device/K052239
Methodology: https://510kreport.com/methodology