Pioneer Surgical Technology, Inc. (Dba Rti Surgical, Inc.)
Pioneer Surgical Technology, Inc. (Dba Rti Surgical, Inc.) holds FDA 510(k) medical device clearances, first cleared 2015, most recent 2020.
Name variants for Pioneer Surgical Technology, Inc. (Dba Rti Surgical, Inc.)
as filed with FDA- Pioneer Surgical Technology, Inc. (Dba Rti Surgical, Inc.)
- Pioneer Surgical Technology, Inc., Dba Rti Surgical, Inc.
Top product codes for Pioneer Surgical Technology, Inc. (Dba Rti Surgical, Inc.)
Recent clearances by Pioneer Surgical Technology, Inc. (Dba Rti Surgical, Inc.)
- K201497 — EVOS Cabling System
- K200095 — Streamline Navigated Instruments
- K193468 — Tritium Sternal Cable Plate System
- K192800 — Streamline TL Spinal Fixation System
- K192718 — Fortilink Interbody Fusion Device (IBF) with TETRAfuse 3D Technology
- K190498 — Fortilink® IBF System with TETRAfuse®3D Technology, include the following designs: Fortilink®-TS IBF System, Fortilink®-L I BF System, Fortilink®-C IBF System
- K183060 — CervAlign Anterior Cervical Plate System
- K172139 — Streamline OCT Occipito-Cervico-Thoracic System
- K170830 — Unison-C Anterior Cervical Fixation System
- K161876 — Tritium® Sternal Cable Plate System
- K161498 — Streamline OCT Occipito-Cervico-Thoracic System
- K153735 — Release Laminoplasty Fixation System
- K152793 — Unison-C Anterior Cervical Fixation System
- K150581 — Tritium Sternal Cable Plate System
- K150254 — Streamline OCT Occipito-Cervico-Thoracic System
Data sourced from openFDA. This site is unofficial and independent of the FDA.