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NuVasive NuvaLine

Page Type
Cleared 510(K)
510(k) Number
K192435
510(k) Type
Traditional
Applicant
NuVasive, Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/26/2019
Days to Decision
21 days
Submission Type
Summary

NuVasive NuvaLine

Page Type
Cleared 510(K)
510(k) Number
K192435
510(k) Type
Traditional
Applicant
NuVasive, Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/26/2019
Days to Decision
21 days
Submission Type
Summary