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FDA 510(k)

Anterior Cervical Plate System

K-Number: K202972 · 2020-11-24

ApplicantNutech Spine and Biologics
Decision Date2020-11-24
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Anterior Cervical Plate System is a medical device manufactured by Nutech Spine and Biologics. It received FDA 510(k) clearance on 2020-11-24 under approval number K202972. 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 Anterior Cervical Plate System?

Anterior Cervical Plate System is a medical device that received FDA 510(k) clearance on 2020-11-24. It is manufactured by Nutech Spine and Biologics. The 510(k) number is K202972.

When was Anterior Cervical Plate System approved by the FDA?

Anterior Cervical Plate System received FDA 510(k) clearance on 2020-11-24, under approval number K202972.

What company makes Anterior Cervical Plate System?

Anterior Cervical Plate System is manufactured by Nutech Spine and Biologics.

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

The FDA product code for 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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