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FDA 510(k)

NuVasive AttraX Scaffold

K-Number: K172497 · 2017-11-24

ApplicantNu Vasive, Incorporated
Decision Date2017-11-24
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

NuVasive AttraX Scaffold is the device name listed in this FDA 510(k) record. The listed applicant is Nu Vasive, Incorporated. It received FDA 510(k) clearance on 2017-11-24 under 510(k) number K172497. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NuVasive AttraX Scaffold?

NuVasive AttraX Scaffold is a medical device that received FDA 510(k) clearance on 2017-11-24. The listed applicant is Nu Vasive, Incorporated. The 510(k) number is K172497.

When did NuVasive AttraX Scaffold receive FDA 510(k) clearance?

NuVasive AttraX Scaffold received FDA 510(k) clearance on 2017-11-24, under 510(k) number K172497.

Who is the listed applicant for NuVasive AttraX Scaffold?

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

What is the FDA product code for NuVasive AttraX Scaffold?

The FDA product code for NuVasive AttraX Scaffold is MQV.

Other records listing Nu Vasive, Incorporated as applicant

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K231735NuVasive CoRoent Small Interbody System; NuVasive CoRoent Small Contoured Interbody System; NuVasive CoRoent Small Interlock System; NuVasive CoRoent Small Interlock II System; NuVasive CoRoent Small Ti-C System; NuVasive Cohere Cervical Interbody SystemK230894NuVasive Modulus ALIF SystemK230989Rod Registration FrameK223181NuVasive Reline SystemK221751NuVasive Cohere ALIF System Intervertebral Body Fusion DeviceK221388NuVasive Reline Cervical System

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Related Devices (Code: MQV)

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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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