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FDA 510(k)

NUVASIVE NEURO VISION SYSTEM

K-Number: K090298 · 2009-06-08

ApplicantNuvasive, Inc.
Decision Date2009-06-08
Product CodeGWF
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NUVASIVE NEURO VISION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Nuvasive, Inc.. It received FDA 510(k) clearance on 2009-06-08 under 510(k) number K090298. The device is classified under product code GWF. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NUVASIVE NEURO VISION SYSTEM?

NUVASIVE NEURO VISION SYSTEM is a medical device that received FDA 510(k) clearance on 2009-06-08. The listed applicant is Nuvasive, Inc.. The 510(k) number is K090298.

When did NUVASIVE NEURO VISION SYSTEM receive FDA 510(k) clearance?

NUVASIVE NEURO VISION SYSTEM received FDA 510(k) clearance on 2009-06-08, under 510(k) number K090298.

Who is the listed applicant for NUVASIVE NEURO VISION SYSTEM?

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 NEURO VISION SYSTEM?

The FDA product code for NUVASIVE NEURO VISION SYSTEM is GWF.

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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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