Bonesupport AB

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K234008CERAMENT GMarch 13, 2024
K240459Cerament Bone Void FillerMarch 5, 2024
DEN210044CERAMENT GMay 17, 2022
K201535Cerament Bone Void FillerOctober 16, 2020
K090871CERAMENT IBONE VOID FILLER HIGH CONTRAST, MODEL A 0210-12September 4, 2009
K073316CERAMENT BONE VOID FILLER, MODEL A0210June 20, 2008
K051951CERAMENT BONE VOID FILLERSeptember 28, 2005