NUVASIVE ANTERIOR LUMBAR 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 Nuvasive Anterior Lumbar Plate System.

Pre-market Notification Details

Device IDK072339
510k NumberK072339
Device Name:NUVASIVE ANTERIOR LUMBAR 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 Received2007-08-20
Decision Date2007-10-19
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
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