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FDA 510(k)

Wolff's Law Anterior Cervical Plate System

K-Number: K240592 · 2024-05-24

Decision Date2024-05-24
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Wolff's Law Anterior Cervical Plate System is a medical device manufactured by Spinal Simplicity, LLC. It received FDA 510(k) clearance on 2024-05-24 under approval number K240592. 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 Wolff's Law Anterior Cervical Plate System?

Wolff's Law Anterior Cervical Plate System is a medical device that received FDA 510(k) clearance on 2024-05-24. It is manufactured by Spinal Simplicity, LLC. The 510(k) number is K240592.

When was Wolff's Law Anterior Cervical Plate System approved by the FDA?

Wolff's Law Anterior Cervical Plate System received FDA 510(k) clearance on 2024-05-24, under approval number K240592.

What company makes Wolff's Law Anterior Cervical Plate System?

Wolff's Law Anterior Cervical Plate System is manufactured by Spinal Simplicity, LLC.

What is the FDA product code for Wolff's Law Anterior Cervical Plate System?

The FDA product code for Wolff's Law Anterior Cervical Plate System is KWQ.

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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.