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NuVasive® Cohere® Thoracolumbar Interbody System

Page Type
Cleared 510(K)
510(k) Number
K200953
510(k) Type
Traditional
Applicant
NuVasive, Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/6/2020
Days to Decision
180 days
Submission Type
Summary

NuVasive® Cohere® Thoracolumbar Interbody System

Page Type
Cleared 510(K)
510(k) Number
K200953
510(k) Type
Traditional
Applicant
NuVasive, Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/6/2020
Days to Decision
180 days
Submission Type
Summary