Detailed description
SpryStep® Plus is designed to help individuals with foot drop syndrome, a condition that makes it difficult to lift the front part of the foot.
This dynamic ankle-foot orthosis (AFO) support features an anterior composite structure that stabilizes the knee and guides it towards extension, particularly benefiting those with weakened plantar flexors by aiding in propulsion and maintaining knee stability during the stance phase.
Key benefits of the SpryStep® Plus include:
- Strategic Stabilization: The composite structure of the SpryStep® Plus offers a balance between flexibility and rigidity, improving walking efficiency and allowing the tibia to tilt during the stance phase.
- Enhanced Mobility: The unique posterior spiral strut design amplifies energy return, helping users move more efficiently.
- Durable Construction: Made from lightweight, durable composite materials with unique laminated characteristics to prevent delamination and breakage.
- Customizable Fit: The trimmable forefoot section ensures an anatomical adjustment allow to fit for various foot sizes and shapes.
- Patient Compliance: The orthosis's elegant design has been developed to provide both comfort and effective support, with the aim of enhancing patient compliance.
- Versatile Use: Suitable for a wide range of patients, from those with mild to pronounced gait abnormalities.
The SpryStep® Plus is available in sizes XS to XL, fitting a broad spectrum of foot sizes. It is offered in both right and left versions to meet individual patient needs. Classified as a Class I medical device, it complies with all relevant regulatory standards.
Cycle-testing independently performed under ISO 10328 Servo-Pneumatic Test System
Patient profile
Adult Neurological
Specifications
Biomechanical deficits of neurological, traumatic or muscular origin.
Weak dorsiflexors.
Fatigueable footdrop.
Footdrop.
Footslap.
Plantar flexor strength =< 3.
Mild spasticity of the foot and ankle.
Partial foot amputation transmetatarsal or more distal.
Mild to moderate knee instability during stance phase.
Mild quadriceps weakness.
Circumduction.
Vaulting (plantarflexion of the contralateral ankle joint).
High knee gait.
Hip hiking/contralateral trunk bending.Do not use the product if the diagnosis has not been confirmed.
Do not apply the product in direct contact with broken skin.
Do not use in the event of known allergy to any of the components.
Do not use for patients weighing > 120 kg (250 lbs).
Severe loss of sensation in the lower limb.
Open ulcers of the foot, ankle or lower leg.
Moderate to severe oedema of the affected limb.
Moderate to severe spasticity of the foot and ankle.
Triplanar instability.
Plantarflexion contracture.
Moderate to severe foot deformities.
Moderate to severe ankle instabilities.
Running/high impact activities.Size Desired length from tip of big toe to heel Shoe size Calf circumference 25 mm below fibula head Size XS 21.5 cm - 24.5 cm 33 cm - 37 cm 29 cm - 37 cm Size S 23 cm - 26 cm 36 cm - 39 cm 32.5 cm - 40 cm Size M 24.5 cm - 27.5 cm 38 cm - 42 cm 35.5 cm - 43 cm Size L 26 cm - 29 cm 41 cm - 44 cm 38.5 cm - 46.5 cm Size XL 29 cm - 30.5 cm 44 cm - 47 cm 42 cm - 49.5 cm Rigid components: carbon fibre - glass fibre - aramid fibre.
Textile components: polyamide - elastane - polyurethane - ethylene vinyl
acetate. Thuasne Deutschland GmbH - Sydney Garden 9 30539 Hannover - Germany
The version of the manual available online is the current version.
Depending on the date of manufacture and place of purchase of the product, this original version of the manual may differ from the version physically present with the product.