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FDA 510(k)

Materialise Shoulder SystemTM Materialise Shoulder Guide and Models SurgiCase Shoulder Planner

K-Number: K220452 · 2022-08-17

Decision Date2022-08-17
Product CodeQHE
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Materialise Shoulder SystemTM Materialise Shoulder Guide and Models SurgiCase Shoulder Planner is a medical device manufactured by Materialise NV. It received FDA 510(k) clearance on 2022-08-17 under approval number K220452. The device is classified under product code QHE. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.