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CODE | PRODUCTION | DESCRIPTION | MATERIAL |
ZK005 | Articulated Minirail Fixator (Vertical Axis) | Whole set | Aluminum |
The vertical axis fixator is typically made of high-quality metal alloys. These alloys are chosen for their durability, enabling the fixator to withstand the mechanical forces it experiences during use and support the bone effectively throughout the treatment period.
The vertical articulation allows for controlled movement specifically in the vertical direction. This controlled movement is designed to aid in the healing process by mimicking the natural movement patterns that are important for the specific orthopedic condition being treated
No, it is suitable for specific fractures where vertical movement is beneficial. It is particularly useful in cases where maintaining some degree of vertical mobility during healing is crucial, such as fractures near joints in the foot or hand.
It is attached to the bone using screws or pins that are carefully inserted into the bone. This attachment method ensures a secure connection between the fixator and the bone, providing the necessary stability for the device to function properly.
While it allows for vertical movement, it may limit some other directions of movement to a certain extent. The main focus is on providing controlled vertical motion, and this can have an impact on the range of motion in other planes depending on the design and how it is adjusted.
There may be some initial discomfort when wearing the fixator, but this can be managed through appropriate medical care, including pain medications and proper positioning adjustments.
Yes, adjustments can be made by a surgeon as needed. The surgeon can modify the degree of vertical articulation based on the progress of the healing process and the specific requirements of the patient's condition.
Possible risks include infection, which can occur with any implanted device, and improper placement. However, these risks can be minimized through proper surgical techniques and post-operative care
The duration it needs to be in place depends on the nature of the injury and the progress of the healing process. The surgeon will monitor the patient's recovery and determine the appropriate time for removal
In some cases, it can be used in combination with other orthopedic devices. This depends on the complexity of the orthopedic condition and whether additional support or functionality is required from other fixators or implants
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