FDA 510(k)

Magnes-C Anterior Cervical Plate System

Numéro K : K221053 · 2023-03-01

DemandeurFellowship of Orthopaedic Researchers, Inc.

Date de décision2023-03-01

Code produitKWQ

Comité consultatifOR

DécisionSubstantially Equivalent

Résumé du dispositif

Magnes-C Anterior Cervical Plate System is the device name listed in this FDA 510(k) record. The listed applicant is Fellowship of Orthopaedic Researchers, Inc.. It received FDA 510(k) clearance on 2023-03-01 under 510(k) number K221053. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Questions fréquentes

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.

Essais cliniques associés

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Dispositifs connexes (Code : KWQ)

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Source officielle

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