MODIFICATION TO NUVASIVE LATERAL PLATE SYSTEM

Appliance, Fixation, Spinal Intervertebral Body

NUVASIVE, INC.

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

Pre-market Notification Details

Device IDK070273
510k NumberK070273
Device Name:MODIFICATION TO NUVASIVE LATERAL PLATE SYSTEM
ClassificationAppliance, Fixation, Spinal Intervertebral Body
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 CodeKWQ  
CFR Regulation Number888.3060 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeSpecial
3rd Party ReviewedNo
Combination ProductNo
Date Received2007-01-29
Decision Date2007-04-03
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
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