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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)
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)
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