# K014189: Odi Talon Intramedullary Hip Nail

- Pathway: 510(k) (Traditional)
- Applicant: Orthopedic Designs, Inc.
- Decided: Mar 21, 2002 after 90 days
- Product code: JDS (Nail, Fixation, Bone)
- 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.
3 later devices descend from it; 2 cite it directly.
0 of 4 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 no predicate by number.

## Most influential descendants
- K033286: Odi Talon Long Proximal Femoral Nail System (2004), 2 descendants of its own
- K111352: Talon Distalfix Proximal Femoral Nail (2011), 1 descendant of its own
- K223933: Exactech Equinoxe PHx Fracture System; Exactech EPIC Screws (2023), 0 descendants of its own

## Indications for use
The ODi Talon™ Intramedullary Hip Nail will be used on indications that are common with presently marketed intramedullary hip nail systems. The primary indications are for fixation/stabilization of stable and unstable fractures of the proximal femur including intertrochanteric fractures, pertrochanteric fractures, high subtrochanteric fractures, and combinations of these fractures. The device is intended to stabilize fragments of the fracture until bony union can occur.

Source page: https://510kreport.com/device/K014189
Methodology: https://510kreport.com/methodology