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NuVasive MOD-EX XLIF Interbody System

Page Type
Cleared 510(K)
510(k) Number
K210439
510(k) Type
Traditional
Applicant
NuVasive, Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/12/2021
Days to Decision
89 days
Submission Type
Summary

NuVasive MOD-EX XLIF Interbody System

Page Type
Cleared 510(K)
510(k) Number
K210439
510(k) Type
Traditional
Applicant
NuVasive, Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/12/2021
Days to Decision
89 days
Submission Type
Summary