Axiomed Freedom Disc -

AxioMed Freedom Disc FDA Approved: NO FDA Indications. Not applicable, it has not been approved for use in the United States by the FDA. Summary. The Freedom Lumbar Disc FLD replaces degenerated lumbar discs using polymer cores designed to. The Freedom Lumbar Disc replacement from AxioMed comprises metal endplates which are porous coated with titanium beads for osteointegration and a viscoelastic polymer silicone polycarbonate urethane polymer articulation. The device is undergoing clinical trials. 20/10/2008 · The Freedom Lumbar Disc is indicated for spinal arthroplasty in skeletally mature patients with single level, symptomatic degenerative disc disease DDD from L3-S1. This is a prospective, multi-center, randomized, controlled trial. Subjects with DDD will be randomized to disc arthroplasty with the FLD device or a control device. AxioMed Freedom™ Disc is a revolutionary cervical and lumbar spinal disc replacement that identically acts like the natural disc because of its patented viscoelastic material. The AxioMed disc has an exclusive, 15-year license to the viscoelastic material, robust IP, in-house manufacturing, and manufacturing trade secrets.

Since its inception, AxioMed has secured over $34M in private equity financing from prestigious venture capitalists. The company´s Freedom® Lumbar Disc has been developed and clinical trials initiated. The company is headed by CEO, Patrick McBrayer, who joined AxioMed in early 2006. Mr. The FLD polymer core is designed to provide the kind of stiffness similar to that found in healthy human discs. Like human discs, the cores are viscoelastic, which means they respond to different loads and loading rates the way a human spine does. Axiomed Spine Corporation. Early Stage Partners co-led the Series A early stage venture capital investment in the life sciences company Axiomed Spine Corporation, which has developed the Freedom Lumbar disc, a second-generation total disc replacement system to restore native function to people with degenerative disc disease, and has continued. 22/02/2019 · The AxioMed Spine Corporation, of Garfield Heights, Ohio, has introduced its Freedom Cervical Disc in Europe and successful implanted its first such device in Switzerland. The firm, which received the CA Mark for it in 2012, developed the total disc replacement device for.

15/12/2015 · Recent clinical studies in Europe examining the AxioMed Freedom total disc replacement technology show favorable results. The studies include: • "Pre-Clinical and Clinical Experience with Viscoelastic Total Disc Replacement" published in SAS Journal 5. 09/01/2013 · Freedom® Cervical Disc Use In The Treatment of Cervical Degenerative Disc Disease The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. The AxioMed viscoelastic disc is a next-generation disc replacement that restores natural disc height, lordosis, stability, and motion in the human spine. AxioMed was approved in September to market and sell their viscoelastic cervical and lumbar Freedom total disc replacements in Australia by the Therapeutic Goods Administration.

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