4WEB receives FDA clearance for anterior lumbar interbody fusion device
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The FDA has granted 510(k) clearance to 4WEB Medical’s stand-alone anterior lumbar interbody fusion device, according to a company press release.
With 4WEB’s Truss mplant echnology, the device eliminates the need for supplemental fixation, according to the release. As screws can be placed directly through the russ implant and into vertebral bodies, the device acts as a stand-alone construct.
“We are excited to add another spine interbody implant to our Truss Implant Technologyportfolio, Jim Bruty, Sr. Vice President of Sales and Marketing, said in the release. The addition of the Stand-Alone Anterior Spine Truss System not only broadens our current offering, but we anticipate this launch to provide significant growth to the organization for the remainder of 2020. 4WEB will continue to stay focused on investments in product development, clinical research, and procedural-based solutions as a means to achieving our long-term growth strategy.”
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