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FDA 510(k)

NUVASIVE MASH

K-Number: K023319 · 2003-03-04

ApplicantNuvasive, Inc.
Decision Date2003-03-04
Product CodeMQP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

NUVASIVE MASH is the device name listed in this FDA 510(k) record. The listed applicant is Nuvasive, Inc.. It received FDA 510(k) clearance on 2003-03-04 under 510(k) number K023319. The device is classified under product code MQP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NUVASIVE MASH?

NUVASIVE MASH is a medical device that received FDA 510(k) clearance on 2003-03-04. The listed applicant is Nuvasive, Inc.. The 510(k) number is K023319.

When did NUVASIVE MASH receive FDA 510(k) clearance?

NUVASIVE MASH received FDA 510(k) clearance on 2003-03-04, under 510(k) number K023319.

Who is the listed applicant for NUVASIVE MASH?

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 MASH?

The FDA product code for NUVASIVE MASH is MQP.

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Other records listing Nuvasive, Inc. as applicant

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Related Devices (Code: MQP)

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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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