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Curiteva Pedicle Screw System

Page Type
Cleared 510(K)
510(k) Number
K191810
510(k) Type
Traditional
Applicant
Curiteva, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/28/2019
Days to Decision
54 days
Submission Type
Summary

Curiteva Pedicle Screw System

Page Type
Cleared 510(K)
510(k) Number
K191810
510(k) Type
Traditional
Applicant
Curiteva, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/28/2019
Days to Decision
54 days
Submission Type
Summary