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Integra® CAPTURE™ Screw System & Integra® Ti6® Internal Fixation System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162153
510(k) Type
Traditional
Applicant
Ascension Orthopedics
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/14/2017
Days to Decision
346 days
Submission Type
Summary

Integra® CAPTURE™ Screw System & Integra® Ti6® Internal Fixation System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162153
510(k) Type
Traditional
Applicant
Ascension Orthopedics
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/14/2017
Days to Decision
346 days
Submission Type
Summary