Comment: In response to our concerns that the aprevo Cervical ACDF System may be appropriately described by C1831, the applicant and a commenter stated that they believe the aprevo Cervical ACDF System meets all the criteria for establishing a new device category and asserted that CMS has used C1831 to describe personalized lumbar interbody fusion devices and that C1831 should not be used to describe the personalized cervical interbody fusion device that is the subject of this transitional pass-through payment application
ProTox-II: A webserver for the prediction of toxicity of chemicals
Ibrahim IA, Shalaby AA, Abd Elaziz RT, Bahr HI
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The opportunity is huge, but the product has to work Even among consumers who are purchasing VMS products after a recommendation from a healthcare provider, product quality and brand reputation are the most frequently important purchase factors
or (B) The Annual Report and Reference Handbook published by the American Board of Medical Specialties, and available from American Board of Medical Specialties, One Rotary Center, Suite 805, Evanston, Illinois 60201
