Magnes-C Anterior Cervical Plate System
K-Number: K221053 · 2023-03-01
Device Summary
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. The listed applicant is Fellowship of Orthopaedic Researchers, Inc.. The 510(k) number is K221053.
When did Magnes-C Anterior Cervical Plate System receive FDA 510(k) clearance?
Magnes-C Anterior Cervical Plate System received FDA 510(k) clearance on 2023-03-01, under 510(k) number K221053.
Who is the listed applicant for Magnes-C Anterior Cervical Plate System?
The FDA 510(k) record lists Fellowship of Orthopaedic Researchers, Inc. as the applicant. This does not by itself establish the device manufacturer.
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.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: KWQ)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.