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This is the dosage recommended in the Physician's Desk Reference (PDR), and the dosage we used in our previous 9-dose study [18]

For the other claims, the applicant provided only background evidence, specifically retrospective studies, which describe findings for a predicate device, the Axoguard Nerve Protector TM , which received FDA 510(k) clearance on January 10, 2014, not the nominated device, the Axoguard HA+ Nerve Protector TM

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What to do when Anthem denies your GLP-1 coverage Denial is not the end