NuVasive® Cohere® Thoracolumbar Interbody System

Intervertebral Fusion Device With Bone Graft, Lumbar

NuVasive, Incorporated

The following data is part of a premarket notification filed by Nuvasive, Incorporated with the FDA for Nuvasive® Cohere® Thoracolumbar Interbody System.

Pre-market Notification Details

Device IDK200953
510k NumberK200953
Device Name:NuVasive® Cohere® Thoracolumbar Interbody System
ClassificationIntervertebral Fusion Device With Bone Graft, Lumbar
Applicant NuVasive, Incorporated 7475 Lusk Blvd. San Diego,  CA  92121
ContactMichelle Cheung
CorrespondentMichelle Cheung
NuVasive, Incorporated 7475 Lusk Blvd. San Diego,  CA  92121
Product CodeMAX  
Subsequent Product CodeOVD
Subsequent Product CodePHM
CFR Regulation Number888.3080 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2020-04-09
Decision Date2020-10-06
Summary:summary

NIH GUDID Devices

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Trademark Results [NuVasive]

Mark Image

Registration | Serial
Company
Trademark
Application Date
NUVASIVE
NUVASIVE
76298757 2818737 Live/Registered
NUVASIVE, INC.
2001-08-10
NUVASIVE
NUVASIVE
75822001 2541247 Live/Registered
NUVASIVE, INC.
1999-10-13

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