Overview
The reprocessed non-sterile external fixation devices are designed for the management of bone fractures and reconstructive, as well as corrective, orthopedic surgery.
The devices are made of metal alloys, plastic, and composites, and are chosen to address a wide range of fractures and applications.
Indications and Contraindications
The devices are indicated for use in patients requiring external skeletal fixation and treatment of fractures, osteotomy, arthrodesis, correction of deformities, fracture revision, bone reconstruction procedures, limb lengthening, and correction of bony or soft tissue deformities and segmental bony or soft tissue defects.
The devices are contraindicated for use in patients with active infections, disabled or non-compliant individuals, and fractures that will heal satisfactorily with conservative treatment.
Warnings and Precautions
The devices are only intended for use by individuals with adequate training and familiarity with techniques associated with the orthopedic surgical procedure employed.
Preoperative frame assembly and adequate supply of components is recommended, and all external fixation devices and components should be inspected prior to surgery.
Manual:
Download: Instructions for Use: Reprocessed Non-Sterile External Fixation Devices
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