FDA 510(k) Applications Submitted by BoneSupport AB

FDA 510(k) Number Submission Date Device Name Applicant
K090871 03/30/2009 CERAMENT IBONE VOID FILLER HIGH CONTRAST, MODEL A 0210-12 BONESUPPORT AB
K073316 11/26/2007 CERAMENT BONE VOID FILLER, MODEL A0210 BONESUPPORT AB
K201535 06/08/2020 Cerament Bone Void Filler BoneSupport AB
DEN210044 09/28/2021 CERAMENT G BoneSupport AB


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