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NuVasive Modulus XLIF Interbody System

Page Type
Cleared 510(K)
510(k) Number
K192760
510(k) Type
Traditional
Applicant
NuVasive, Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/2019
Days to Decision
18 days
Submission Type
Summary

NuVasive Modulus XLIF Interbody System

Page Type
Cleared 510(K)
510(k) Number
K192760
510(k) Type
Traditional
Applicant
NuVasive, Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/2019
Days to Decision
18 days
Submission Type
Summary