FDA 510(k) Applications Submitted by Pioneer Surgical Technology, Inc. (DBA RTI Surgical, Inc.)
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K183060 |
11/02/2018 |
CervAlignÖ Anterior Cervical Plate System |
Pioneer Surgical Technology, Inc. (DBA RTI Surgical, Inc.) |
| K192800 |
09/30/2019 |
Streamline TL Spinal Fixation System |
Pioneer Surgical Technology, Inc. (DBA RTI Surgical, Inc.) |
| K193468 |
12/16/2019 |
Tritium Sternal Cable Plate System |
Pioneer Surgical Technology, Inc. (dba RTI Surgical, Inc.) |
| K150254 |
02/03/2015 |
Streamline OCT Occipito-Cervico-Thoracic System |
Pioneer Surgical Technology, Inc. (DBA RTI Surgical, Inc.) |
| K150581 |
03/09/2015 |
Tritium Sternal Cable Plate System |
Pioneer Surgical Technology, Inc. (DBA RTI Surgical, Inc.) |
| K161498 |
06/01/2016 |
Streamline OCT Occipito-Cervico-Thoracic System |
Pioneer Surgical Technology, Inc. (DBA RTI Surgical, Inc.) |
| K201497 |
06/05/2020 |
EVOS Cabling System |
Pioneer Surgical Technology, Inc. (DBA RTI Surgical, Inc.) |
| K172139 |
07/17/2017 |
Streamline OCT Occipito-Cervico-Thoracic System |
Pioneer Surgical Technology, Inc. (DBA RTI Surgical, Inc.) |
| K153735 |
12/28/2015 |
Release Laminoplasty Fixation System |
Pioneer Surgical Technology, Inc. (DBA RTI Surgical, Inc.) |
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