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NuVasive NuvaLine Mobile App

Page Type
Cleared 510(K)
510(k) Number
K162647
510(k) Type
Traditional
Applicant
NUVASIVE, INCORPORATED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/2017
Days to Decision
221 days
Submission Type
Summary

NuVasive NuvaLine Mobile App

Page Type
Cleared 510(K)
510(k) Number
K162647
510(k) Type
Traditional
Applicant
NUVASIVE, INCORPORATED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/2017
Days to Decision
221 days
Submission Type
Summary