NUVASIVE HELIX-T ACP 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 Helix-t Acp System.

Pre-market Notification Details

Device IDK083341
510k NumberK083341
Device Name:NUVASIVE HELIX-T ACP SYSTEM
ClassificationAppliance, Fixation, Spinal Intervertebral Body
Applicant NUVASIVE, INC. 7475 LUSK BLVD San Diego,  CA  92121
ContactHan Fan
CorrespondentHan Fan
NUVASIVE, INC. 7475 LUSK BLVD San Diego,  CA  92121
Product CodeKWQ  
CFR Regulation Number888.3060 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeSpecial
3rd Party ReviewedNo
Combination ProductNo
Date Received2008-11-12
Decision Date2009-03-20
Summary:summary

NIH GUDID Devices

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