Pioneer Surgical Technology, Inc. (Dba Rti Surgical, Inc.)

FDA Regulatory Profile

Pioneer Surgical Technology, Inc. (Dba Rti Surgical, Inc.) has 0 FDA recalls, 0 inspections, 16 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Oct 28, 2020

Updated: recalls Oct 23, 2026 · inspections Oct 23, 2026 · compliance actions Oct 23, 2026.

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Summary

Recalls
0
510(k) Clearances
16
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K201497EVOS Cabling SystemOct 28, 2020
K200513DAC Dynamic Active Compression PlateJul 22, 2020
K200095Streamline Navigated InstrumentsJun 26, 2020
K193468Tritium Sternal Cable Plate SystemMar 12, 2020
K192800Streamline TL Spinal Fixation SystemJan 14, 2020
K192718Fortilink Interbody Fusion Device (IBF) with TETRAfuse 3D TechnologyDec 20, 2019
K190498Fortilink® IBF System with TETRAfuse®3D Technology, include the following designs: Fortilink®-TS IBF…Jul 5, 2019
K183060CervAlign™ Anterior Cervical Plate SystemJan 17, 2019
K172139Streamline OCT Occipito-Cervico-Thoracic SystemAug 18, 2017
K170830Unison-C Anterior Cervical Fixation SystemJun 28, 2017
K161876Tritium® Sternal Cable Plate SystemSep 9, 2016
K161498Streamline OCT Occipito-Cervico-Thoracic SystemAug 22, 2016
K153735Release Laminoplasty Fixation SystemJan 21, 2016
K152793Unison-C Anterior Cervical Fixation SystemJan 19, 2016
K150581Tritium Sternal Cable Plate SystemJun 4, 2015
K150254Streamline OCT Occipito-Cervico-Thoracic SystemApr 28, 2015