Osartis GmbH

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K240856Hip Spacer Molds; Knee Spacer Molds; Shoulder Spacer MoldsNovember 20, 2024
K202458BonOs Inject, Pedicle screw kits, Cement pusherMay 18, 2021
K210120BonOs HV, BonOs MV, BonOs LVMarch 19, 2021
K210125BonOs HV Genta, BonOs MV Genta, BonOs LV GentaMarch 19, 2021
K192394Hi-Fatigue Bone CementDecember 2, 2019
K192379Hi-Fatigue G Bone CementNovember 27, 2019