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Curiteva Lumbar Interbody Fusion System

Page Type
Cleared 510(K)
510(k) Number
K181589
510(k) Type
Traditional
Applicant
Curiteva, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/2018
Days to Decision
185 days
Submission Type
Summary

Curiteva Lumbar Interbody Fusion System

Page Type
Cleared 510(K)
510(k) Number
K181589
510(k) Type
Traditional
Applicant
Curiteva, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/2018
Days to Decision
185 days
Submission Type
Summary