FDA 510(k)

NuVasive Modulus ALIF System

K-Number: K210271 · 2021-03-01

Decision Date2021-03-01

Product CodeOVD

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

NuVasive Modulus ALIF System is a medical device manufactured by Nu Vasive, Incorporated. It received FDA 510(k) clearance on 2021-03-01 under approval number K210271. 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 Modulus ALIF System?

NuVasive Modulus ALIF System is a medical device that received FDA 510(k) clearance on 2021-03-01. It is manufactured by Nu Vasive, Incorporated. The 510(k) number is K210271.

When was NuVasive Modulus ALIF System approved by the FDA?

NuVasive Modulus ALIF System received FDA 510(k) clearance on 2021-03-01, under approval number K210271.

What company makes NuVasive Modulus ALIF System?

NuVasive Modulus ALIF System is manufactured by Nu Vasive, Incorporated.

What is the FDA product code for NuVasive Modulus ALIF System?

The FDA product code for NuVasive Modulus ALIF System is OVD.

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.