Pioneer Surgical Technology, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pioneer Surgical Technology, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Resolve Anterior Cervical Plate System, CODA™ Anterior Cervical Plate System, CervAlign® Anterior Cervical Plate System
27
Total
27
Cleared
0
Denied
Pioneer Surgical Technology, Inc. has 27 FDA 510(k) cleared orthopedic devices. Based in Marquette, US.
Latest FDA clearance: Jul 2026. Active since 2010.
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) Regulatory Record - Pioneer Surgical Technology, Inc.
27 devices
Cleared
Jul 16, 2026
Cable-Ready® Cable Grip System
Orthopedic
90d
Cleared
Jul 11, 2025
Resolve Anterior Cervical Plate System
Orthopedic
64d
Cleared
Nov 18, 2022
CODA™ Anterior Cervical Plate System
Orthopedic
92d
Cleared
Jun 23, 2021
CervAlign® Anterior Cervical Plate System
Orthopedic
48d
Cleared
Nov 26, 2019
Streamline MIS Spinal Fixation System
Orthopedic
84d
Cleared
Apr 10, 2014
STREAMLINE TL SPINAL FIXATION SYSTEM
Orthopedic
22d
Cleared
Mar 27, 2014
CROSSFUSE II CORONAL TAPER, CROSSFUSE II HYPERLORDOTIC
Orthopedic
135d
Cleared
Feb 10, 2014
C-PLUS
Orthopedic
76d
Cleared
Feb 07, 2014
NB3D BONE VOID FILLER
Orthopedic
220d
Cleared
Jan 27, 2014
TRITIUM STERNAL CABLE PLATE SYSTEM
Orthopedic
46d
Cleared
Dec 24, 2013
PIONEER MAXFUSE VERTEBRAL BODY REPLACEMENT DEVICE
Orthopedic
195d
Cleared
Jun 27, 2013
STREAMLINE TL SPINAL SYSTEM
Orthopedic
69d