NuVasive® Precept™ Spinal System

Thoracolumbosacral Pedicle Screw System

NuVasive, Incorporated

The following data is part of a premarket notification filed by Nuvasive, Incorporated with the FDA for Nuvasive® Precept™ Spinal System.

Pre-market Notification Details

Device IDK171894
510k NumberK171894
Device Name:NuVasive® Precept™ Spinal System
ClassificationThoracolumbosacral Pedicle Screw System
Applicant NuVasive, Incorporated 7475 Lusk Blvd. San Diego,  CA  92121
ContactMarysa Loustalot
CorrespondentMarysa E. Loustalot
NuVasive, Incorporated 7475 Lusk Boulevard San Diego,  CA  92121
Product CodeNKB  
Subsequent Product CodeKWP
Subsequent Product CodeKWQ
CFR Regulation Number888.3070 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2017-06-26
Decision Date2017-09-28
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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