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FDA 510(k)

APTUS® Forearm Shaft Plates and APTUS® Wrist 2.5 System

K-Number: K193554 · 2020-02-16

ApplicantMedartis AG
Decision Date2020-02-16
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

APTUS® Forearm Shaft Plates and APTUS® Wrist 2.5 System is a medical device manufactured by Medartis AG. It received FDA 510(k) clearance on 2020-02-16 under approval number K193554. 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 APTUS® Forearm Shaft Plates and APTUS® Wrist 2.5 System?

APTUS® Forearm Shaft Plates and APTUS® Wrist 2.5 System is a medical device that received FDA 510(k) clearance on 2020-02-16. It is manufactured by Medartis AG. The 510(k) number is K193554.

When was APTUS® Forearm Shaft Plates and APTUS® Wrist 2.5 System approved by the FDA?

APTUS® Forearm Shaft Plates and APTUS® Wrist 2.5 System received FDA 510(k) clearance on 2020-02-16, under approval number K193554.

What company makes APTUS® Forearm Shaft Plates and APTUS® Wrist 2.5 System?

APTUS® Forearm Shaft Plates and APTUS® Wrist 2.5 System is manufactured by Medartis AG.

What is the FDA product code for APTUS® Forearm Shaft Plates and APTUS® Wrist 2.5 System?

The FDA product code for APTUS® Forearm Shaft Plates and APTUS® Wrist 2.5 System is HRS.

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Other Devices by Medartis AG

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Related Devices (Code: HRS)

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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.

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