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NuVaisve® Reline® Cervical System

Page Type
Cleared 510(K)
510(k) Number
K191553
510(k) Type
Traditional
Applicant
NuVasive, Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/14/2019
Days to Decision
63 days
Submission Type
Summary

NuVaisve® Reline® Cervical System

Page Type
Cleared 510(K)
510(k) Number
K191553
510(k) Type
Traditional
Applicant
NuVasive, Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/14/2019
Days to Decision
63 days
Submission Type
Summary