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# Ossiofiber Compression Screw Portfolio Cleared
- URL: https://www.fdaweb.com/ossiofiber-compression-screw-portfolio-cleared/
- Published: 2020-10-19T12:00:00.000Z
- Updated: 2026-09-14T16:33:04.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5147901

FDA has cleared an Ossio 510(k) for its Ossio*fiber* Compression Screw Portfolio for alignment maintenance and fixation of bone fractures, comminuted fractures, fragments, osteotomies, arthrodesis and bone grafts of the upper extremity, fibula, knee, ankle and foot. The devices comprise a 4.0mm-diameter cannulated, headless, partially threaded compression screw in lengths ranging from 26mm to 60mm, according to the company. It says that studies show that implants made from Ossio*fiber* provide easy insertion and secure fixation with rapid bone attachment in as little as two weeks following surgery, and gradual, safe incorporation and complete integration into the surrounding anatomy within 18 to 24 months.