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FDA 510(k)

NuVasive AttraX Scaffold

K-Number: K240507 · 2024-03-20

ApplicantNuvasive, Inc.
Decision Date2024-03-20
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

NuVasive AttraX Scaffold is a medical device manufactured by Nuvasive, Inc.. It received FDA 510(k) clearance on 2024-03-20 under approval number K240507. 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 2024-03-20. It is manufactured by Nuvasive, Inc.. The 510(k) number is K240507.

When was NuVasive AttraX Scaffold approved by the FDA?

NuVasive AttraX Scaffold received FDA 510(k) clearance on 2024-03-20, under approval number K240507.

What company makes NuVasive AttraX Scaffold?

NuVasive AttraX Scaffold is manufactured by Nuvasive, Inc..

What is the FDA product code for NuVasive AttraX Scaffold?

The FDA product code for NuVasive AttraX Scaffold is MQV.

Other Devices by Nuvasive, Inc.

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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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