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FDA 510(k)

NuVasive BASE Interfixated Titanium System

K-Number: K170592 · 2017-04-26

ApplicantNu Vasive, Incorporated
Decision Date2017-04-26
Product CodeOVD
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

NuVasive BASE Interfixated Titanium System is a medical device manufactured by Nu Vasive, Incorporated. It received FDA 510(k) clearance on 2017-04-26 under approval number K170592. 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 BASE Interfixated Titanium System?

NuVasive BASE Interfixated Titanium System is a medical device that received FDA 510(k) clearance on 2017-04-26. It is manufactured by Nu Vasive, Incorporated. The 510(k) number is K170592.

When was NuVasive BASE Interfixated Titanium System approved by the FDA?

NuVasive BASE Interfixated Titanium System received FDA 510(k) clearance on 2017-04-26, under approval number K170592.

What company makes NuVasive BASE Interfixated Titanium System?

NuVasive BASE Interfixated Titanium System is manufactured by Nu Vasive, Incorporated.

What is the FDA product code for NuVasive BASE Interfixated Titanium System?

The FDA product code for NuVasive BASE Interfixated Titanium System is OVD.

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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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