FDA 510(k) Applications Submitted by Karin Darle Olsson

FDA 510(k) Number Submission Date Device Name Applicant
K150669 03/16/2015 Neoss TiBase, Neoss CoCr Abutments (Mono and Multi) Neoss Ltd
K143327 11/20/2014 Neoss Ti Reinforced Membrane Neoss Ltd


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