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
K240459	02/16/2024	Cerament Bone Void Filler	Bonesupport AB
K201535	06/08/2020	Cerament Bone Void Filler	BoneSupport AB
DEN210044	09/28/2021	CERAMENT G	BoneSupport AB
K234008	12/19/2023	CERAMENT G	BoneSupport AB