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FDA 510(k)

Belvedere™ Lateral Plating System

K-Number: K153097 · 2016-07-15

ApplicantNeurostructures, Inc.
Decision Date2016-07-15
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Belvedere™ Lateral Plating System is the device name listed in this FDA 510(k) record. The listed applicant is Neurostructures, Inc.. It received FDA 510(k) clearance on 2016-07-15 under 510(k) number K153097. 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 Belvedere™ Lateral Plating System?

Belvedere™ Lateral Plating System is a medical device that received FDA 510(k) clearance on 2016-07-15. The listed applicant is Neurostructures, Inc.. The 510(k) number is K153097.

When did Belvedere™ Lateral Plating System receive FDA 510(k) clearance?

Belvedere™ Lateral Plating System received FDA 510(k) clearance on 2016-07-15, under 510(k) number K153097.

Who is the listed applicant for Belvedere™ Lateral Plating System?

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

What is the FDA product code for Belvedere™ Lateral Plating System?

The FDA product code for Belvedere™ Lateral Plating System is KWQ.

Other records listing Neurostructures, Inc. as applicant

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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.

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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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