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NuVasive Reline System

Page Type
Cleared 510(K)
510(k) Number
K223181
510(k) Type
Traditional
Applicant
NuVasive, Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/11/2023
Days to Decision
92 days
Submission Type
Summary

NuVasive Reline System

Page Type
Cleared 510(K)
510(k) Number
K223181
510(k) Type
Traditional
Applicant
NuVasive, Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/11/2023
Days to Decision
92 days
Submission Type
Summary