NuVasive® XLX Interbody System
K-Number: K173892 · 2018-05-04
ApplicantNu Vasive, Incorporated
Decision Date2018-05-04
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
NuVasive® XLX Interbody System is a medical device manufactured by Nu Vasive, Incorporated. It received FDA 510(k) clearance on 2018-05-04 under approval number K173892. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the NuVasive® XLX Interbody System?
NuVasive® XLX Interbody System is a medical device that received FDA 510(k) clearance on 2018-05-04. It is manufactured by Nu Vasive, Incorporated. The 510(k) number is K173892.
When was NuVasive® XLX Interbody System approved by the FDA?
NuVasive® XLX Interbody System received FDA 510(k) clearance on 2018-05-04, under approval number K173892.
What company makes NuVasive® XLX Interbody System?
NuVasive® XLX Interbody System is manufactured by Nu Vasive, Incorporated.
What is the FDA product code for NuVasive® XLX Interbody System?
The FDA product code for NuVasive® XLX Interbody System is MAX.
Related Clinical Trials
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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.