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NuVasive Reline Cervical System

Page Type
Cleared 510(K)
510(k) Number
K221388
510(k) Type
Traditional
Applicant
NuVasive, Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/2022
Days to Decision
119 days
Submission Type
Summary

NuVasive Reline Cervical System

Page Type
Cleared 510(K)
510(k) Number
K221388
510(k) Type
Traditional
Applicant
NuVasive, Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/2022
Days to Decision
119 days
Submission Type
Summary