Advertise With UsAdvertise on our extensive network of industry websites and newsletters.
Get the PBR newsletterSign up to our free email to get all the latest PBR
news.Amedica, an orthopedic and spinal implants company, has received the FDA 510(k) marketing clearance for the company's SEEplate cervical plate system.
Subscribe to our email newsletter
The SEEplate cervical plate system incorporates features that are aimed at allowing surgeons an alternative to confirming the secure placement of the anti-back-out mechanism of screws used as part of the spinal implant system.
The SEEplate cervical plate system is intended for anterior screw fixation of cervical spine from the C2 through C7 vertebral bodies of the spine as an adjunct to cervical spine fusion.
Ashok Khandkar, CEO of Amedica, said: “FDA clearance of our SEEplate cervical plate system is another important milestone for Amedica. This cervical plate system will complement our line of innovative, silicon nitride ceramic spinal spacers, providing surgeons and patients with an important new option for spinal fixation.”