FH Orthopedics has received FDA clearance for the CoLS PEEK fixation screws for use during the CoLS technique for tendon graft fixation to the femur and tibia during ACL and PCL reconstruction, according to a company news release.
The device is a non-metal option for fixation, which means the implant won't set off metal detectors in airports or negatively impact MRIs. The device has been used with almost 20,000 patients worldwide.
The device is designed to reduce postoperative laxity.
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The device is designed to reduce postoperative laxity.
Related Articles on Orthopedic Devices:
Exactech Reports 21% Decline in 4Q Spine & Biologics Sales
Eden Spine Receives FDA Clearance for Corpectomy Device
Innovation Medical Device Solutions Opens New Orlando Facility