Tyber Medical has received U.S. Food and Drug Administration 510(k) clearance for its headless cannulated trauma screw system.
Here are three things to know about the company and the device:
1. The system allows users to choose from a broad range of trauma screw sizes. These screws are indicated for use throughout the human body in bone reconstruction, osteotomy, arthrodesis, joint fusion, fracture repair and fracture fixation.
"This 510(k) clearance adds over 9,000 devices to our growing product portfolio," said Stu Shank, Tyber Medical's sales manager.
2. Tyber Medical's products also include the Tyber Medical Interbody System ALIF, PLIF, TLIF, DLIF, which received FDA 510(k) clearance in September 2013.
3. Tyber Medical is a private label original equipment manufacturer and it is focused on designing and developing full class II orthopedic systems.
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