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Tyber Medical issued 510(k) clearance for trauma screw system

Tyber Medical recently announced it has received FDA 510(k) clearance for a new headless cannulated trauma screw system.

Indicated for use in bone reconstruction, osteotomy, arthrodesis, joint fusion and fracture fixation, the screws come in a range of sizes from 1.5 mm to 9 mm in diameter. They have a titanium or stainless steel body with short, long or full threads and come in either sterile or non-sterile packing. The screws are self-drilling and self-tapping and are available in either Torx or hex connection.

“This 510(k) clearance adds over 9,000 devices to our growing product portfolio,” Stu Shank, Tyber Medical sales manager, said in a company press release. “Tyber Medical’s broad selection will allow our customers to differentiate themselves by offering the correct screw size for each indication.”