OSSIO, Inc., an orthopedic fixation technology company, today announced that its OSSIOfiber Compression Screw Portfolio has received 510(k) market clearance from the U.S. Food and Drug Administration (FDA) for maintenance of alignment and fixation of bone fractures, comminuted fractures, fragments, osteotomies, arthrodesis and bone grafts of the upper extremity, fibula, knee, ankle and foot in the presence of appropriate brace and/or immobilization.

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Source: https://blog.ourcrowd.com/ossio-announces-u-s-launch-and-first-commercial-use-of-the-ossiofiber-trimmable-fixation-nail-system-for-broad-utilization-in-foot-ankle-and-hand-wrist-procedures-2/