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FDA 510(k)

Magnes-C Anterior Cervical Plate System

K-Number: K221053 · 2023-03-01

ApplicantFellowship of Orthopaedic Researchers, Inc.
Decision Date2023-03-01
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Magnes-C Anterior Cervical Plate System is a medical device manufactured by Fellowship of Orthopaedic Researchers, Inc.. It received FDA 510(k) clearance on 2023-03-01 under approval number K221053. 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 Magnes-C Anterior Cervical Plate System?

Magnes-C Anterior Cervical Plate System is a medical device that received FDA 510(k) clearance on 2023-03-01. It is manufactured by Fellowship of Orthopaedic Researchers, Inc.. The 510(k) number is K221053.

When was Magnes-C Anterior Cervical Plate System approved by the FDA?

Magnes-C Anterior Cervical Plate System received FDA 510(k) clearance on 2023-03-01, under approval number K221053.

What company makes Magnes-C Anterior Cervical Plate System?

Magnes-C Anterior Cervical Plate System is manufactured by Fellowship of Orthopaedic Researchers, Inc..

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

The FDA product code for Magnes-C Anterior Cervical Plate System is 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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