Pioneer Surgical Technology, Inc. (Dba Rti Surgical, Inc.) - FDA 510(...
15
Total
15
Cleared
0
Denied
Pioneer Surgical Technology, Inc. (Dba Rti Surgical, Inc.) has 15 FDA 510(k) cleared orthopedic devices. Based in Marquette, US.
Historical record: 15 cleared submissions from 2015 to 2020.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Pioneer Surgical Technology, Inc....
15 devices
Cleared
Oct 28, 2020
EVOS Cabling System
Orthopedic
145d
Cleared
Jun 26, 2020
Streamline Navigated Instruments
Orthopedic
162d
Cleared
Mar 12, 2020
Tritium Sternal Cable Plate System
Orthopedic
87d
Cleared
Jan 14, 2020
Streamline TL Spinal Fixation System
Orthopedic
106d
Cleared
Dec 20, 2019
Fortilink Interbody Fusion Device (IBF) with TETRAfuse 3D Technology
Orthopedic
84d
Cleared
Jul 05, 2019
Fortilink® IBF System with TETRAfuse®3D Technology, include the following...
Orthopedic
127d
Cleared
Jan 17, 2019
CervAlign™ Anterior Cervical Plate System
Orthopedic
76d
Cleared
Aug 18, 2017
Streamline OCT Occipito-Cervico-Thoracic System
Orthopedic
32d
Cleared
Jun 28, 2017
Unison-C Anterior Cervical Fixation System
Orthopedic
100d
Cleared
Sep 09, 2016
Tritium® Sternal Cable Plate System
Orthopedic
63d
Cleared
Aug 22, 2016
Streamline OCT Occipito-Cervico-Thoracic System
Orthopedic
82d
Cleared
Jan 21, 2016
Release Laminoplasty Fixation System
Orthopedic
24d
Cleared
Jan 19, 2016
Unison-C Anterior Cervical Fixation System
Orthopedic
113d
Cleared
Jun 04, 2015
Tritium Sternal Cable Plate System
Orthopedic
87d
Cleared
Apr 28, 2015
Streamline OCT Occipito-Cervico-Thoracic System
Orthopedic
84d