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We invite public comments on whether the Transdermal GFR Measurement System utilizing Lumitrace meets the cost criterion and our proposal to approve new technology add-on payments for Transdermal GFR Measurement System utilizing Lumitrace for FY 2024 subject to the technology receiving FDA marketing authorization as a Breakthrough Device for the indication corresponding to the Breakthrough Device designation by July 1, 2023

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doi: 10.5603/EP.a2021.0074

less self-mutilation of the denervated limb, a proxy for restored sensation), microscopic/morphometric (faster axonal regeneration, better-organized neural fascicles, increased density and size of regenerating fibers, and epineural/perineural regeneration), and functional (electromyography and walking recovery via the sciatic functional index)

NaBPC157 did not cause any tissue or organ damage