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NuVasive LessRay with Enhanced Tracking

Page Type
Cleared 510(K)
510(k) Number
K170800
510(k) Type
Traditional
Applicant
NuVasive, Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/18/2017
Days to Decision
154 days
Submission Type
Summary

NuVasive LessRay with Enhanced Tracking

Page Type
Cleared 510(K)
510(k) Number
K170800
510(k) Type
Traditional
Applicant
NuVasive, Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/18/2017
Days to Decision
154 days
Submission Type
Summary