Stryker Corporation has announced that it has received U.S. Food and Drug Administration (FDA) 510(k) clearance for its Incompass® Total Ankle System. This new implant is designed for patients with ankle joints damaged by severe rheumatoid, post-traumatic, or degenerative arthritis. The Incompass system integrates advanced technologies from Stryker's existing Inbone® and Infinity® systems into a comprehensive solution for total ankle replacement. Developed using the Stryker Orthopaedic Modeling & Analytics (SOMA) platform, the system offers improved surgical flexibility and efficiency, leveraging data from extensive clinical cases and CT scans.
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