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Fortilink Interbody Fusion Device (IBF) with TETRAfuse 3D Technology

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K192718
510(k) Type
Traditional
Applicant
Pioneer Surgical Technology, Inc., DBA RTI Surgical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/2019
Days to Decision
84 days
Submission Type
Summary

Fortilink Interbody Fusion Device (IBF) with TETRAfuse 3D Technology

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K192718
510(k) Type
Traditional
Applicant
Pioneer Surgical Technology, Inc., DBA RTI Surgical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/2019
Days to Decision
84 days
Submission Type
Summary