Last synced on 30 May 2025 at 11:05 pm

Tritium® Sternal Cable Plate System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K161876
510(k) Type
Special
Applicant
Pioneer Surgical Technology, Inc. DBA RTI Surgical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/2016
Days to Decision
63 days
Submission Type
Summary

Tritium® Sternal Cable Plate System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K161876
510(k) Type
Special
Applicant
Pioneer Surgical Technology, Inc. DBA RTI Surgical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/2016
Days to Decision
63 days
Submission Type
Summary