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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 the device name listed in this FDA 510(k) record. The listed applicant is Nuvasive, Inc.. It received FDA 510(k) clearance on 2024-03-20 under 510(k) 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. The listed applicant is Nuvasive, Inc.. The 510(k) number is K240507.

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

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

Who is the listed applicant for NuVasive AttraX Scaffold?

The FDA 510(k) record lists Nuvasive, Inc. 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.

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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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