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A review of some basic biomechanical principles that were used in the design of the Prestige® Cervical Disc.
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Date:
January 07, 2009
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The authors report the results of a prospective randomized multicenter study in which the results of cervical disc arthroplasty were compared with anterior cervical discectomy and fusion (ACDF) in patients treated for symptomatic single-level cervical degenerative disc disease (DDD).
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Date:
January 07, 2009
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In this article from the Journal of Neurosurgery, range of motion (ROM) changes were evaluated at the surgically treated and adjacent segments in cadaveric specimens treated with two different cervical artificial discs compared with those measured in intact spine and fusion models.
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Date:
January 07, 2009
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The PRESTIGE® Cervical Disc is a stainless steel surgical implant indicated to treat patients suffering from degenerative disc disease (DDD) of the cervical (neck) spine.
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Date:
January 07, 2009
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Ionics Medical Corporation announced that the company has received FDA clearance to market the Dyn-ALIF intervertebral body spinal fusion device. The device mimics the shock-absorbing features of the natural disc and is vertically expandable to provide a precise fit for a wide range of disc space heights.
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Company:
Date:
November 20, 2008
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Medtronic, Inc. announced today that it has received U.S. Food and Drug Administration (FDA) approval to market the PRESTIGE® Cervical Disc, the first artificial disc commercially available in the U.S. for use in the neck.
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Company:
Date:
January 07, 2009
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An anterior cervical fixation system for degenerative and trauma conditions
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Company:
Date:
October 20, 2008
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The 9300XSP is the brightest light source available. Visualize more clearly, see color more accurately, and work more effectively.
300W Xenon Lamp Outshines Metal Halide and Halogen Lamps
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Company:
Date:
July 17, 2008
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Superior Processing• Validated in vitro assay to confirm the osteoinductivity of each DBM lot• Sterile - product is e-beam sterilized Each lot of DBM used to create Accell technology passes a validated in vitro assay, ensuring osteoinductivity.
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Company:
Date:
July 22, 2008
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With its family of Accell products, IsoTis has introduced a new class of bone graft substitutes that is much more powerful than the majority of other bone graft substitutes being used in orthopedic surgery today.
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Company:
Date:
June 05, 2008
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