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FDA 510(k) Applications Submitted by Pioneer Surgical Technology, Inc., DBA RTI Surgical, Inc.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K192718
09/27/2019
Fortilink Interbody Fusion Device (IBF) with TETRAfuse 3D Technology
Pioneer Surgical Technology, Inc., DBA RTI Surgical, Inc.
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