FDA 510(k) Applications Submitted by Sarah Pleaugh
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| 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.) |
| K170830 |
03/20/2017 |
Unison-C Anterior Cervical Fixation 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.) |
| K161876 |
07/08/2016 |
Tritium« Sternal Cable Plate 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.) |
| K213351 |
10/08/2021 |
ds Head 32ch 3.0T |
Invivo Corporation (Business Trade Name: Philips) |
| K153735 |
12/28/2015 |
Release Laminoplasty Fixation System |
Pioneer Surgical Technology, Inc. (DBA RTI Surgical, Inc.) |
|
|
