NuVasive® Modulus TLIF Interbody System
K-Number: K172341 · 2017-10-26
Device Summary
Frequently Asked Questions
What is the NuVasive® Modulus TLIF Interbody System?
NuVasive® Modulus TLIF Interbody System is a medical device that received FDA 510(k) clearance on 2017-10-26. It is manufactured by Nu Vasive, Incorporated. The 510(k) number is K172341.
When was NuVasive® Modulus TLIF Interbody System approved by the FDA?
NuVasive® Modulus TLIF Interbody System received FDA 510(k) clearance on 2017-10-26, under approval number K172341.
What company makes NuVasive® Modulus TLIF Interbody System?
NuVasive® Modulus TLIF Interbody System is manufactured by Nu Vasive, Incorporated.
What is the FDA product code for NuVasive® Modulus TLIF Interbody System?
The FDA product code for NuVasive® Modulus TLIF 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.