Ossio Earns 510(k) Clearance for Compression-Screw Products

Ossio has received 510(k) marketing clearance from the FDA for its OSSIOfiber compression- screw family of products for bone alignment and fixation.

The clearance allows the implants to be used for aligning and fixating fractures, fragments and bone grafts in the upper extremity, fibula, knee, ankle and foot.

The implants show rapid bone attachment in as little as two weeks after surgery and complete integration within 18 to 24 months, the company said.