Materialise Shoulder SystemTM Materialise Shoulder Guide and Models SurgiCase Shoulder Planner
K-Number: K220452 · 2022-08-17
Device Summary
Frequently Asked Questions
What is the Materialise Shoulder SystemTM Materialise Shoulder Guide and Models SurgiCase Shoulder Planner?
Materialise Shoulder SystemTM Materialise Shoulder Guide and Models SurgiCase Shoulder Planner is a medical device that received FDA 510(k) clearance on 2022-08-17. It is manufactured by Materialise NV. The 510(k) number is K220452.
When was Materialise Shoulder SystemTM Materialise Shoulder Guide and Models SurgiCase Shoulder Planner approved by the FDA?
Materialise Shoulder SystemTM Materialise Shoulder Guide and Models SurgiCase Shoulder Planner received FDA 510(k) clearance on 2022-08-17, under approval number K220452.
What company makes Materialise Shoulder SystemTM Materialise Shoulder Guide and Models SurgiCase Shoulder Planner?
Materialise Shoulder SystemTM Materialise Shoulder Guide and Models SurgiCase Shoulder Planner is manufactured by Materialise NV.
What is the FDA product code for Materialise Shoulder SystemTM Materialise Shoulder Guide and Models SurgiCase Shoulder Planner?
The FDA product code for Materialise Shoulder SystemTM Materialise Shoulder Guide and Models SurgiCase Shoulder Planner is QHE.
Related Clinical Trials
Other Devices by Materialise NV
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.