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FDA 510(k)

NuVasive Brigade Lateral System

K-Number: K181386 · 2018-08-24

ApplicantNu Vasive, Incorporated
Decision Date2018-08-24
Product CodeOVD
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

NuVasive Brigade Lateral System is a medical device manufactured by Nu Vasive, Incorporated. It received FDA 510(k) clearance on 2018-08-24 under approval number K181386. The device is classified under product code OVD. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NuVasive Brigade Lateral System?

NuVasive Brigade Lateral System is a medical device that received FDA 510(k) clearance on 2018-08-24. It is manufactured by Nu Vasive, Incorporated. The 510(k) number is K181386.

When was NuVasive Brigade Lateral System approved by the FDA?

NuVasive Brigade Lateral System received FDA 510(k) clearance on 2018-08-24, under approval number K181386.

What company makes NuVasive Brigade Lateral System?

NuVasive Brigade Lateral System is manufactured by Nu Vasive, Incorporated.

What is the FDA product code for NuVasive Brigade Lateral System?

The FDA product code for NuVasive Brigade Lateral System is OVD.

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Other Devices by Nu Vasive, Incorporated

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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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