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Three-dimensional micro-computed tomographic imaging of alveolar bone in experimental bone loss or repair
The skin is a target organ, not an obstacle
or (2) for devices for which pass-through status will begin on or after January 1, 2020, as an alternative to the substantial clinical improvement criterion, the device is part of the FDA's Breakthrough Devices Program and has received FDA marketing authorization for the indication covered by the Breakthrough Device designation
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Zum anderen muss auch gewhrleistet sein, dass sich keine unerwnschten Bakterien und Keime im Produkt ausbreiten
Annu Rev Nutr 1999;19:357-77
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