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FDA 510(k)

Origin™ Anterior Cervical Plate System

K-Number: K193494 · 2020-04-06

ApplicantOrthopaedic & Spine Development
Decision Date2020-04-06
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Origin™ Anterior Cervical Plate System is a medical device manufactured by Orthopaedic & Spine Development. It received FDA 510(k) clearance on 2020-04-06 under approval number K193494. 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 Origin™ Anterior Cervical Plate System?

Origin™ Anterior Cervical Plate System is a medical device that received FDA 510(k) clearance on 2020-04-06. It is manufactured by Orthopaedic & Spine Development. The 510(k) number is K193494.

When was Origin™ Anterior Cervical Plate System approved by the FDA?

Origin™ Anterior Cervical Plate System received FDA 510(k) clearance on 2020-04-06, under approval number K193494.

What company makes Origin™ Anterior Cervical Plate System?

Origin™ Anterior Cervical Plate System is manufactured by Orthopaedic & Spine Development.

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

The FDA product code for Origin™ 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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