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FDA 510(k)

NuVasive® Modulus-C Interbody System

K-Number: K172676 · 2017-12-14

ApplicantNu Vasive, Incorporated
Decision Date2017-12-14
Product CodeODP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

NuVasive® Modulus-C Interbody System is a medical device manufactured by Nu Vasive, Incorporated. It received FDA 510(k) clearance on 2017-12-14 under approval number K172676. The device is classified under product code ODP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NuVasive® Modulus-C Interbody System?

NuVasive® Modulus-C Interbody System is a medical device that received FDA 510(k) clearance on 2017-12-14. It is manufactured by Nu Vasive, Incorporated. The 510(k) number is K172676.

When was NuVasive® Modulus-C Interbody System approved by the FDA?

NuVasive® Modulus-C Interbody System received FDA 510(k) clearance on 2017-12-14, under approval number K172676.

What company makes NuVasive® Modulus-C Interbody System?

NuVasive® Modulus-C Interbody System is manufactured by Nu Vasive, Incorporated.

What is the FDA product code for NuVasive® Modulus-C Interbody System?

The FDA product code for NuVasive® Modulus-C Interbody System is ODP.

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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.

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