Last synced on 25 April 2025 at 11:05 pm

Curiteva Pedicle Screw System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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