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FDA 510(k)

Skyway Anterior Cervical Plate System

K-Number: K243015 · 2024-11-05

ApplicantKyocera Medical Technologies, Inc.
Decision Date2024-11-05
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Skyway Anterior Cervical Plate System is a medical device manufactured by Kyocera Medical Technologies, Inc.. It received FDA 510(k) clearance on 2024-11-05 under approval number K243015. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Skyway Anterior Cervical Plate System?

Skyway Anterior Cervical Plate System is a medical device that received FDA 510(k) clearance on 2024-11-05. It is manufactured by Kyocera Medical Technologies, Inc.. The 510(k) number is K243015.

When was Skyway Anterior Cervical Plate System approved by the FDA?

Skyway Anterior Cervical Plate System received FDA 510(k) clearance on 2024-11-05, under approval number K243015.

What company makes Skyway Anterior Cervical Plate System?

Skyway Anterior Cervical Plate System is manufactured by Kyocera Medical Technologies, Inc..

What is the FDA product code for Skyway Anterior Cervical Plate System?

The FDA product code for Skyway Anterior Cervical Plate System is KWQ.

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Related Devices (Code: KWQ)

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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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