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AOD-9604s lack of IGF-1 impact may make it more appropriate for individuals with these concerns, though individual medical evaluation remains essential

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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

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