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In the United States (US), the Oxford Partial Knee is intended for use in individuals with osteoarthritis or avascular necrosis limited to the medial compartment of the knee and is intended to be implanted with bone cement; it is not indicated for use in the lateral compartment or for patients with ligament deficiency. Potential risks include, but are not limited to, loosening, dislocation, fracture, wear, and infection, any of which can require additional surgery. For complete prescribing information, see the package insert and www.zimmerbiomet.com.
Various countries outside of the US offer Oxford partial knees intended for lateral use and Oxford Partial Knees with cementless application; these devices are not available for sale in the US. Check for local product clearances and reference product specific instructions for use.
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