NuVasive Modulus XLIF Interbody System
K-Number: K163230 · 2017-03-16
Device Summary
Frequently Asked Questions
What is the NuVasive Modulus XLIF Interbody System?
NuVasive Modulus XLIF Interbody System is a medical device that received FDA 510(k) clearance on 2017-03-16. It is manufactured by Nu Vasive, Incorporated. The 510(k) number is K163230.
When was NuVasive Modulus XLIF Interbody System approved by the FDA?
NuVasive Modulus XLIF Interbody System received FDA 510(k) clearance on 2017-03-16, under approval number K163230.
What company makes NuVasive Modulus XLIF Interbody System?
NuVasive Modulus XLIF Interbody System is manufactured by Nu Vasive, Incorporated.
What is the FDA product code for NuVasive Modulus XLIF Interbody System?
The FDA product code for NuVasive Modulus XLIF Interbody System is MAX.
Related Clinical Trials
Other Devices by Nu Vasive, Incorporated
Related Devices (Code: MAX)
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.