Last synced on 14 November 2025 at 11:06 pm

NuVasive® VersaTie System

Page Type
Cleared 510(K)
510(k) Number
K161265
510(k) Type
Traditional
Applicant
NUVASIVE, INCORPORATED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/15/2016
Days to Decision
71 days
Submission Type
Summary

NuVasive® VersaTie System

Page Type
Cleared 510(K)
510(k) Number
K161265
510(k) Type
Traditional
Applicant
NUVASIVE, INCORPORATED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/15/2016
Days to Decision
71 days
Submission Type
Summary