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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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