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NuVasive BASE Interfixated Titanium System

Page Type
Cleared 510(K)
510(k) Number
K170592
510(k) Type
Traditional
Applicant
NuVasive, Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/26/2017
Days to Decision
57 days
Submission Type
Summary

NuVasive BASE Interfixated Titanium System

Page Type
Cleared 510(K)
510(k) Number
K170592
510(k) Type
Traditional
Applicant
NuVasive, Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/26/2017
Days to Decision
57 days
Submission Type
Summary