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NuVasive® Modulus TLIF Interbody System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172341
510(k) Type
Traditional
Applicant
Nu Vasive, Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/26/2017
Days to Decision
85 days
Submission Type
Summary

NuVasive® Modulus TLIF Interbody System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172341
510(k) Type
Traditional
Applicant
Nu Vasive, Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/26/2017
Days to Decision
85 days
Submission Type
Summary