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NuVasive Cohere Thoracolumbar Interbody System

Page Type
Cleared 510(K)
510(k) Number
K181860
510(k) Type
Traditional
Applicant
NuVasive, Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/5/2018
Days to Decision
85 days
Submission Type
Summary

NuVasive Cohere Thoracolumbar Interbody System

Page Type
Cleared 510(K)
510(k) Number
K181860
510(k) Type
Traditional
Applicant
NuVasive, Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/5/2018
Days to Decision
85 days
Submission Type
Summary