Osartis GmbH

Osartis GmbH holds 6 FDA 510(k) medical device clearances, first cleared 2019, most recent 2024.

Top product codes for Osartis GmbH

LOD — Orthopedic5 devices
MBB — Orthopedic1 device

Recent clearances by Osartis GmbH

K240856 — Hip Spacer Molds; Knee Spacer Molds; Shoulder Spacer MoldsCode MBB·2024-11-20
K202458 — BonOs Inject, Pedicle screw kits, Cement pusherCode LOD·2021-05-18
K210120 — BonOs HV, BonOs MV, BonOs LVCode LOD·2021-03-19
K210125 — BonOs HV Genta, BonOs MV Genta, BonOs LV GentaCode LOD·2021-03-19
K192394 — Hi-Fatigue Bone CementCode LOD·2019-12-02
K192379 — Hi-Fatigue G Bone CementCode LOD·2019-11-27

Data sourced from openFDA. This site is unofficial and independent of the FDA.