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Fortilink® IBF System with TETRAfuse®3D Technology, include the following designs: Fortilink®-TS IBF System, Fortilink®-L I BF System, Fortilink®-C IBF System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190498
510(k) Type
Traditional
Applicant
Pioneer Surgical Technology, Inc. DBA RTI Surgical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/5/2019
Days to Decision
127 days
Submission Type
Summary

Fortilink® IBF System with TETRAfuse®3D Technology, include the following designs: Fortilink®-TS IBF System, Fortilink®-L I BF System, Fortilink®-C IBF System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190498
510(k) Type
Traditional
Applicant
Pioneer Surgical Technology, Inc. DBA RTI Surgical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/5/2019
Days to Decision
127 days
Submission Type
Summary