# K142602: VALOR Hindfoot Fusion Nail System

- Pathway: 510(k) (Special)
- Applicant: Wrightmedicaltechnologyinc
- Decided: Oct 22, 2014 after 37 days
- Product code: HSB (Rod, Fixation, Intramedullary And Accessories)
- Device class: 2
- Regulation: 21 CFR 888.3020
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K090857 (2009). 1 ancestor in all.
1 later device descends 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)
- K090857: Valor Ankle Fusion Nail System, Wrightmedicaltechnologyinc (2009) Summary page 4.

## Most influential descendants
- K221031: Arthrex DualCompression Hindfoot Fusion Nail Implant System (2022), 0 descendants of its own

## Indications for use
The VALOR® Hindfoot Fusion Nail System is intended to facilitate tibiotalocalcaneal arthrodesis in any of the following indications: » Severe foot/ankle deformity, * Osteoarthritis, « Instability and skeletal defects after tumor resection, * Neuro-arthropathic deformity or Charcot deformity, « Avascular necrosis of the talus, « Revision of a failed joint replacement or failed ankle fusion, « Distal tibia fracture and non-unions, » Rheumatoid arthritis and pseudoarthosis

Source page: https://510kreport.com/device/K142602
Methodology: https://510kreport.com/methodology