NuVasive Navigation Instruments

Orthopedic Stereotaxic Instrument

NuVasive, Incorporated

The following data is part of a premarket notification filed by Nuvasive, Incorporated with the FDA for Nuvasive Navigation Instruments.

Pre-market Notification Details

Device IDK172623
510k NumberK172623
Device Name:NuVasive Navigation Instruments
ClassificationOrthopedic Stereotaxic Instrument
Applicant NuVasive, Incorporated 7475 Lusk Blvd. San Diego,  CA  92121
ContactManthan J. Damani
CorrespondentManthan J. Damani
NuVasive, Incorporated 7475 Lusk Blvd. San Diego,  CA  92121
Product CodeOLO  
CFR Regulation Number882.4560 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2017-09-01
Decision Date2017-12-21
Summary:summary

NIH GUDID Devices

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