




Healthcare Industry News: dysphagia
News Release - April 24, 2012
LDR Announces FDA Clearance and Launch of the ROI-C(R) Lordotic Cervical Cage
ROI-C Lordotic Cervical Cage expands LDR’s market-leading stand-alone cervical fusion portfolio featuring VerteBRIDGE® Plating TechnologyAUSTIN, Texas--(Healthcare Sales & Marketing Network)--LDR, a privately held medical device company offering innovative spinal implants for both non-fusion and fusion applications, announced that it has received 510(k) clearance from the United States Food and Drug Administration to market the ROI-C Lordotic Cervical Cage. The ROI-C Lordotic Cervical Cage adds to the company’s market leading stand-alone portfolio and compliments the existing ROI-C anatomically shaped cage introduced in 2009. When used with the company’s integrated VerteBRIDGE® plating technology, both cages offer a zero profile, stand-alone construct for fusion in the cervical spine. The design of the ROI-C Lordotic Cervical Cage provides an additional option during surgery allowing surgeons to treat patients with more varied anatomy and reduces the need for thick cervical plates that may contribute to dysphagia, or difficulty swallowing.
Christophe Lavigne, President and CEO of LDR, comments, “We are excited to strengthen our worldwide leadership in stand-alone device innovation by introducing the ROI-C Lordotic Cervical Cage into the U.S. market. LDR has led the way in providing surgeons with a broad selection of implant geometries for stand-alone cervical and lumbar fusions. The ROI-C Lordotic Cervical Cage represents the latest application of VerteBRIDGE Plating technology which has been successfully used in more than 25,000 cervical and lumbar cage implantations worldwide since 2008.”
Dr. Robert Jackson, Chief of Neurosurgery at Mission Hospital Regional Medical Center and Assistant Clinical Professor of Neurosurgery at the University of California Irvine, implanted the first ROI-C Lordotic Cervical Cage in the United States and shares the company’s enthusiasm about the product, “A critical aspect of anterior cervical fusion is providing excellent stability through good bone-implant contact and primary stability with immediate loading. That is best achieved by matching the cage to a patient’s specific anatomy. LDR has acknowledged and addressed these challenges with an innovative addition to its product line to address more varied anatomies. LDR’s cervical offering addresses the anatomical challenges I encounter and allows me to deliver better care to my patients.”
LDR was founded in 2000 by partners Christophe Lavigne, Hervé Dinville, and Patrick Richard in Troyes, France. Currently headquartered in Austin, TX, LDR has experienced rapid growth through product portfolio expansion and an increasingly global presence. LDR develops unique implantable spine devices and instrumentation designed to support the clinical goals of surgery while making procedures easier to perform. More information is located at www.ldrholding.com.
©2012 LDR Holding Corporation, All Rights Reserved
Source: LDR Spine
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