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    Pioneer Surgical Technology Inc.

    Manufacturer
    🇺🇸 United States

    Pioneer Surgical Technology, Inc.

    FDA registration
    Pioneer Surgical Technology, Inc.·43 products·🇺🇸 United States

    PIONEER SURGICAL TECHNOLOGY QUANTUM SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PIONEER SURGICAL TECHNOLOGY QUANTUM SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PIONEER SURGICAL TECHNOLOGY EXTENDED GTR, MODEL 501-601

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MODIFICATION TO: PIONEER SURGICAL TECHNOLOGY QUANTUM SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PIONEER SURGICAL RELEASE LAMINOPLASTY FIXATION SYSTEM, STEAM STERILIZATION CASE

    FDA Adverse Event
    Malfunction ·PIONEER SURGICAL TECHNOLOGY (D.B.A.RTI SURGICAL)·Product code LRP·October 18, 2016

    PIONEER SURGICAL TECHNOLOGY FORTILINK C

    FDA Adverse Event
    Death ·PIONEER SURGICAL TECHNOLOGY·Product code MAX·September 17, 2021

    PIONEER SURGICAL TECHNOLOGY NANOSS BVF-E, MODELS 5, 10, 20CC

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PIONEER SURGICAL TECHNOLOGY (D.B.A. RTI SURGICAL) STERNAL CABLE SYSTEM

    FDA Adverse Event
    Injury ·PIONEER SURGICAL TECHNOLOGY (D.B.A. RTI SURGICAL)·Product code JDQ·March 10, 2017

    PIONEER SURGICAL TECHNOLOGY CONTRACT ANTERIOR LUMBAR PLATE SCREW TIGHTENER

    FDA Adverse Event
    Malfunction ·PIONEER SURGICAL TECHNOLOGY (D.B.A. RTI SURGICAL)·Product code LXH·January 3, 2017

    PIONEER SURGICAL TECHNOLOGY (D.B.A. RTI SURGICAL) STERNAL CABLE SYSTEM

    FDA Adverse Event
    Injury ·PIONEER SURGICAL TECHNOLOGY (D.B.A. RTI SURGICAL)·Product code JDQ·March 10, 2017

    STREAMLINE OCT OCCIPITO CERVICO THORACIC SYSTEM

    FDA Adverse Event
    Injury ·PIONEER SURGICAL TECHNOLOGY (D.B.A. RTI SURGICAL)·Product code KWP·July 12, 2016

    STREAMLINE OCT NAVIGATED INSTRUMENTS

    FDA Adverse Event
    Malfunction ·PIONEER SURGICAL (D.B.A. RTI SURGICAL)·Product code OLO·October 2, 2020

    PIONEER SURGICAL'S STREAMLINE MIS THREADED SCREW INSERTER

    FDA Adverse Event
    Malfunction ·PIONEER SURGICAL TECHNOLOGY (D.B.A. RTI SURGICAL)·Product code NKB·March 30, 2017

    STAY FUSE

    FDA Adverse Event
    Other ·NEXA ORTHOPEDICS·Product code KWH·September 6, 2006

    1.7MM CABLE WITH CRIMP 750MM-STERILE

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code JDQ·December 12, 2018

    UNKNOWN SCREWS

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SàRL CH·Product code HWC·February 1, 2024

    PIONEER SURGICAL TECHNOLOGY

    FDA Adverse Event
    Injury ·PIONEER SURGICAL TECHNOLOGY·Product code NKB·May 18, 2023

    PIONEER SURGICAL TECHNOLOGY

    FDA Adverse Event
    Injury ·PIONEER SURGICAL TECHNOLOGY·Product code NKB·May 18, 2023