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FDA 510(k)

IXOS Radius Plate System

K-Number: K171624 · 2018-03-29

ApplicantStuckenbrock Medizintechnik GmbH
Decision Date2018-03-29
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

IXOS Radius Plate System is a medical device manufactured by Stuckenbrock Medizintechnik GmbH. It received FDA 510(k) clearance on 2018-03-29 under approval number K171624. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IXOS Radius Plate System?

IXOS Radius Plate System is a medical device that received FDA 510(k) clearance on 2018-03-29. It is manufactured by Stuckenbrock Medizintechnik GmbH. The 510(k) number is K171624.

When was IXOS Radius Plate System approved by the FDA?

IXOS Radius Plate System received FDA 510(k) clearance on 2018-03-29, under approval number K171624.

What company makes IXOS Radius Plate System?

IXOS Radius Plate System is manufactured by Stuckenbrock Medizintechnik GmbH.

What is the FDA product code for IXOS Radius Plate System?

The FDA product code for IXOS Radius Plate System is HRS.

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Official Source

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