CS002SL Chopart Foot Plate

This 100% carbon keel is designed to be a flexible and durable solution for the longest amputation levels and partial foot prostheses. Includes a 10mm heel height for compatibility with standard FlexFoot shells and low-heel shoes. Chopart is specifically designed for people with chopart amputations as well as lisfranc, pirogoff, boyd and partial foot prostheses.

Proportional response
The layering of carbon fiber optimizes the deflection of the forefoot from mid-stance to toe-off and is proportional to the user’s weight and impact level.

Full length toe lever
The full-length keel/toe lever matches the length of the sound foot, giving a smoother, symmetrical gait.

Waterproof
Whether it's fresh water, salt water or chlorinated water, Waterproof Össur pro ducts will give you the maximum protection you need. The use of first-rate materials provides permanent protection against harmful ingress of water, even after submersion, whilst continuing to provide the functionality you expect.

CLINICAL Instruction
DESCRIPTION

• The device consists of a single carbon blade for direct lamination (Fig. 1). This device must be used with a Foot Cover and a Spectra Sock.

INTENDED USE

• The device is intended as a part of a prosthetic system that replaces the foot and ankle function of a missing lower limb.
• Suitability of the device for the prosthesis and the patient must be evaluated by a healthcare professional. The device must be fitted and adjusted by a healthcare professional.

Indications For Use and Target Patient Population

• Lower limb amputation and/or congenital deficiency
• No known contraindications
• The device is for low to high impact use, e.g., walking and occasional running.

GENERAL SAFETY INSTRUCTIONS

• The healthcare professional should inform the patient about everything in this document that is required for safe use of this device.
• Warning: If there is a change or loss in device functionality, or if the device shows signs of damage or wear hindering its normal functions, the patient should stop using the device and contact a healthcare professional.
• The device is for single patient use.