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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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