Last synced on 14 November 2025 at 11:06 pm

NuVasive Anterior Cervical Plate Systems

Page Type
Cleared 510(K)
510(k) Number
K212446
510(k) Type
Traditional
Applicant
NuVasive, Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/3/2021
Days to Decision
90 days
Submission Type
Summary

NuVasive Anterior Cervical Plate Systems

Page Type
Cleared 510(K)
510(k) Number
K212446
510(k) Type
Traditional
Applicant
NuVasive, Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/3/2021
Days to Decision
90 days
Submission Type
Summary