# K071395: Biomet Vision Footring System

- Pathway: 510(k) (Traditional)
- Applicant: Biomet Manufacturing Corp
- Decided: Jul 9, 2007 after 49 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 K831576 (1983). 4 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K052239: Ebi Dynafix Vision Footplate System, Ebi, L.P. (2005) Summary page 1.
- K944092: Additional Accessories for the Orthofix System, Orthofix Srl (1995) Summary page 1.
- K955848: Orthofix Modulsystem, Orthofix, Inc. (1996) Summary page 1.
- (no number) Biomet® Vision® FootRing System: named in the summary without a submission number

## Most influential descendants
- K093753: Mdpo Frame System (2010), 0 descendants of its own

## Indications for use
The Biomet® Vision® FootRing System is intended for use in the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by the use of the external fixation treatment modality.

Source page: https://510kreport.com/device/K071395
Methodology: https://510kreport.com/methodology