MODIFICATION TO NUVASIVE NEUROVISION JJB SYSTEM

Stimulator, Electrical, Evoked Response

NUVASIVE, INC.

The following data is part of a premarket notification filed by Nuvasive, Inc. with the FDA for Modification To Nuvasive Neurovision Jjb System.

Pre-market Notification Details

Device IDK062765
510k NumberK062765
Device Name:MODIFICATION TO NUVASIVE NEUROVISION JJB SYSTEM
ClassificationStimulator, Electrical, Evoked Response
Applicant NUVASIVE, INC. 4545 TOWNE CENTRE COURT San Diego,  CA  92121
ContactLaetitia Cousin
CorrespondentLaetitia Cousin
NUVASIVE, INC. 4545 TOWNE CENTRE COURT San Diego,  CA  92121
Product CodeGWF  
CFR Regulation Number882.1870 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeSpecial
3rd Party ReviewedNo
Combination ProductNo
Date Received2006-09-29
Decision Date2007-01-24
Summary:summary

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