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FDA 510(k)

MODIFICATION TO: NUVASIVE NEUROVISION JJB SYSTEM

K-Number: K051384 · 2005-07-11

ApplicantNuvasive, Inc.
Decision Date2005-07-11
Product CodeGWF
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO: NUVASIVE NEUROVISION JJB 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 2005-07-11 under 510(k) number K051384. 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 MODIFICATION TO: NUVASIVE NEUROVISION JJB SYSTEM?

MODIFICATION TO: NUVASIVE NEUROVISION JJB SYSTEM is a medical device that received FDA 510(k) clearance on 2005-07-11. The listed applicant is Nuvasive, Inc.. The 510(k) number is K051384.

When did MODIFICATION TO: NUVASIVE NEUROVISION JJB SYSTEM receive FDA 510(k) clearance?

MODIFICATION TO: NUVASIVE NEUROVISION JJB SYSTEM received FDA 510(k) clearance on 2005-07-11, under 510(k) number K051384.

Who is the listed applicant for MODIFICATION TO: NUVASIVE NEUROVISION JJB 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 MODIFICATION TO: NUVASIVE NEUROVISION JJB SYSTEM?

The FDA product code for MODIFICATION TO: NUVASIVE NEUROVISION JJB SYSTEM is GWF.

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Other records listing Nuvasive, Inc. as applicant

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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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