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FDA 510(k)

Quantum Anterior Cervical Plate

K-Number: K210424 · 2021-10-22

ApplicantNvision Biomedical Technologies, Inc.
Decision Date2021-10-22
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Quantum Anterior Cervical Plate is the device name listed in this FDA 510(k) record. The listed applicant is Nvision Biomedical Technologies, Inc.. It received FDA 510(k) clearance on 2021-10-22 under 510(k) number K210424. 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 Quantum Anterior Cervical Plate?

Quantum Anterior Cervical Plate is a medical device that received FDA 510(k) clearance on 2021-10-22. The listed applicant is Nvision Biomedical Technologies, Inc.. The 510(k) number is K210424.

When did Quantum Anterior Cervical Plate receive FDA 510(k) clearance?

Quantum Anterior Cervical Plate received FDA 510(k) clearance on 2021-10-22, under 510(k) number K210424.

Who is the listed applicant for Quantum Anterior Cervical Plate?

The FDA 510(k) record lists Nvision Biomedical Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Quantum Anterior Cervical Plate?

The FDA product code for Quantum Anterior Cervical Plate 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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