# K103015: Odrc-Dynamic Hip Screw System

- Pathway: 510(k) (Traditional)
- Applicant: Orthopaedic Device Research Center
- Decided: Apr 13, 2011 after 183 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: 1 generation back to K981757 (1998). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K981757: Synthes (Usa) DHS Helix System, Synthes (Usa) (1998) Summary page 1.

## Indications for use
The ODRC-DHS System is intended for use in fixation of fractures to the proximal femur. The system is indicated for use in trochanteric, pertrochanteric, intertrochanteric, and basilar neck fractures.

Source page: https://510kreport.com/device/K103015
Methodology: https://510kreport.com/methodology