NuVasive Navigation Instruments
K-Number: K172623 · 2017-12-21
ApplicantNu Vasive, Incorporated
Decision Date2017-12-21
Product CodeOLO
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
NuVasive Navigation Instruments is a medical device manufactured by Nu Vasive, Incorporated. It received FDA 510(k) clearance on 2017-12-21 under approval number K172623. The device is classified under product code OLO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the NuVasive Navigation Instruments?
NuVasive Navigation Instruments is a medical device that received FDA 510(k) clearance on 2017-12-21. It is manufactured by Nu Vasive, Incorporated. The 510(k) number is K172623.
When was NuVasive Navigation Instruments approved by the FDA?
NuVasive Navigation Instruments received FDA 510(k) clearance on 2017-12-21, under approval number K172623.
What company makes NuVasive Navigation Instruments?
NuVasive Navigation Instruments is manufactured by Nu Vasive, Incorporated.
What is the FDA product code for NuVasive Navigation Instruments?
The FDA product code for NuVasive Navigation Instruments is OLO.
Related Clinical Trials
Other Devices by Nu Vasive, Incorporated
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.