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FDA 510(k)

Liberty Anterior Cervical Plate

K-Number: K172585 · 2017-10-23

ApplicantValorus Spine
Decision Date2017-10-23
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Liberty Anterior Cervical Plate is a medical device manufactured by Valorus Spine. It received FDA 510(k) clearance on 2017-10-23 under approval number K172585. 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 Liberty Anterior Cervical Plate?

Liberty Anterior Cervical Plate is a medical device that received FDA 510(k) clearance on 2017-10-23. It is manufactured by Valorus Spine. The 510(k) number is K172585.

When was Liberty Anterior Cervical Plate approved by the FDA?

Liberty Anterior Cervical Plate received FDA 510(k) clearance on 2017-10-23, under approval number K172585.

What company makes Liberty Anterior Cervical Plate?

Liberty Anterior Cervical Plate is manufactured by Valorus Spine.

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

The FDA product code for Liberty Anterior Cervical Plate is KWQ.

Related Clinical Trials

Other Devices by Valorus Spine

Related Devices (Code: KWQ)

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.