FDA 510(k) Applications Submitted by Christoph Ulrich

FDA 510(k) Number Submission Date Device Name Applicant
K150650 03/12/2015 neon3 ULRICH GMBH & CO. KG
K161032 04/13/2016 neon3Ö universal OCT spinal stabilization ULRICH GMBH & CO. KG
K052385 08/30/2005 TANGORS POLYAXIAL SYSTEM ULRICH GMBH & CO. KG


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