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FDA 510(k) Applications Submitted by ARTOSS GMBH
FDA 510(k) Number
Submission Date
Device Name
Applicant
K190110
01/23/2019
NanoBone SBX PUTTY, NanoBone QD
Artoss Gmbh
K141189
05/08/2014
NANOBONE / GRANULATE
ARTOSS GMBH
K161351
05/16/2016
NanoBone SBX Putty
ARTOSS GMBH
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