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Charcot neuroarthropathy, or Charcot foot and ankle, is a condition that occurs in patients with abnormal sensation (neuropathy). It is a progressive deformity that occurs with minimal trauma. Bone destruction and eventual resportion occurs, which can lead to profound deformity.
Intramedullary nailing system
An intramedullary nailing system indicated for internal bone fixation of the foot for neuropathic osteoarthropathy (Charcot), fracture fixation, osteotomies, non-unions, mal-unions, and fusions. Instrumentation designed for accurate nail insertion.
This system focuses on treating cases such as neuropathic deformity requiring arthrodesis of the medial and lateral columns, with or without corrective osteotomies. Patients with poor quality, soft bone (e.g. Charcot), require implants specifically designed to deliver strength and maintain purchase in these difficult cases. S indicated for fixation of fractures, osteotomies, reconstruction procedures, non-unions, and fusions of bones in the foot and ankle including the Metatarsals, Cuneiforms, Cuboid, Navicular, Calcaneus and Talus. Specific examples include: Intramedullary Medial Column Fusion, Lateral Column Fusion and Subtalar Fusions resulting from neuropathic osteoarthropathy (Charcot). Wright Medical - Stryker
External Fixation System
Designed to address fractures, nonunion, and complex foot and ankle deformities including Charcot neuroarthropathy. The system may be used for definitive treatment as the sole fixation device or used in conjunction with the Salvation Beams and Bolts or the Salvation 3Di Plating System. Salvation External Fixation - Stryker - Wright Medical Group
Salvation Fusion Bolts and Beams - Wright Medical Group Stryker - Indicated for fracture fixation, osteotomies, reconstruction procedures, non-unions, and fusions of bones in the foot and ankle including the Metatarsals, Cuneiforms, Cuboid, Navicular, Calcaneus and Talus. Specific examples include Medial Column Fusion and Lateral Column Fusion resulting from neuropathic osteoarthropathy (Charcot).
The ankle includes the tibia, talus and the fibula bones.
Injectable Bone Substitute
An injectable, self-setting bone substitute composed of tetra-calcium phosphate that is formulated to convert to hydroxyapatite, the principal mineral component of bone.
Plating platform
The Anchorage CP plating system is a single-use bone fixation appliance intended to be permanently implanted. They are designed with different shaped plates made of bio compatible titanium.
Memometal nitinol implant
The EasyClip memometal nitinol implant has a low profile and dynamic compression. It is a superelastic staple fixation system.
Headless compression screws
The Fixos screw system is a single use device intended for the fixation, correction or stabilization of small and long bones available in 4.0mm, 5.0mm and 7.0mm headless screw sizes.
Screw system
The Asnis III cannulated screws have a low profile head, self drilling and self tapping design and a long drill bit.
Salvation Plating
Salvation 3Di Plating System is designed to address the unique demands of advanced midfoot reconstruction. The system focuses on treating cases such as neuropathic deformity requiring arthrodesis of the medial column, with or without corrective osteotomies. Stryker - Wright Medical Group
Plating system
The Stryker Anchorage 2 CP system is intended for use in internal fixation, reconstruction and treatment of fractures in the foot and ankle in adult and adolescent patients.
Plating platform
Locking plate system for reconstruction or arthrodesis of small bones, including the fore, mid- and hind foot and ankle.
Dedicated to the foot and ankle surgeon.
As one of the world’s leading companies in medical technology, Stryker is dedicated to helping foot and ankle surgeons treat their patients more efficiently while enhancing patient care and the overall healthcare experience. Constantly driven to innovate, we offer a diverse array of advanced medical technologies and a comprehensive portfolio of products. We’re here for the foot and ankle surgeon. We’re here to make healthcare better.
Circular External Fixation System
Circular external fixation for fractures, joint contractures, fusions, limb lengthening, deformity correction and bone and soft tissue reconstruction in pediatric patients and adults.
Augment is the first and only FDA approved alternative to autograft in hindfoot and ankle arthrodesis backed by the largest prospective Level 1 RCT in Foot and Ankle Orthopedic history. In the randomized, controlled pivotal trial conducted to support U.S. FDA approval of Augment Bone Graft, 75% of the treated patients had one or more risk factors for non-union. Literature reports a range of 10% to as high as 41% of all hindfoot and ankle fusions fail.