Pioneer Surgical Technology, Inc. (Dba Rti Surgical, Inc.)
FDA 510(k) & PMA Approved Devices — 7 products
Total Devices7
Categories5
Latest Approval2020-10-28
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K201497 | EVOS Cabling System | JDQ | 2020-10-28 | View |
| 510(k) | K193468 | Tritium Sternal Cable Plate System | JDQ | 2020-03-12 | View |
| 510(k) | K192800 | Streamline TL Spinal Fixation System | NKB | 2020-01-14 | View |
| 510(k) | K183060 | CervAlign Anterior Cervical Plate System | KWQ | 2019-01-17 | View |
| 510(k) | K172139 | Streamline OCT Occipito-Cervico-Thoracic System | NKG | 2017-08-18 | View |
| 510(k) | K161498 | Streamline OCT Occipito-Cervico-Thoracic System | NKG | 2016-08-22 | View |
| 510(k) | K153735 | Release Laminoplasty Fixation System | NQW | 2016-01-21 | View |
No matching devices.