Home GUDID 07640387660423 GoPLF! Posterior Lateral Fusion Device
Primary DI 07640387660423
Brand GoPLF! Posterior Lateral Fusion Device
Company GetSet Surgical SA
Model 3205540
Device description GoPLF! Posterior Lateral Fusion Device, 2 Screws, Multi-Axial Titanium Screw, 5.5 x 40mm
Published 2022-02-21
Public version status New
Distribution status In Commercial Distribution
MRI safety MR Conditional
Rx true
OTC false
Sterile true
Single use true Product Codes# Code, Name table Code Name NKB Thoracolumbosacral Pedicle Screw System
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class NKB Thoracolumbosacral Pedicle Screw System Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 07640387660010 Primary GS1 0 07640387660423 Unit of Use GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, EAN-13 table Source identifier GTIN-14 normalized EAN-13 07640387660010 07640387660010 7640387660010 07640387660423 07640387660423 7640387660423
GMDN Terms# Term, Definition table Term Definition Bone-screw internal spinal fixation system, sterile An assembly of sterile implantable devices intended to provide immobilization and stabilization of spinal segments in the treatment of various spinal instabilities or deformities, also used as an adjunct to spinal fusion [e.g., for degenerative disc disease (DDD)]. Otherwise known as a pedicle screw instrumentation system, it typically consists of a combination of anchors (e.g., bolts, hooks, pedicle screws or other types), interconnection mechanisms (incorporating nuts, screws, sleeves, or bolts), longitudinal members (e.g., plates, rods, plate/rod combinations), and/or transverse connectors. Sterile disposable devices associated with implantation may be included.
Regulatory Flags# DUNS number 480143831 Device count 2 DM exempt false Premarket exempt false HCT/P false Kit false Combination product false Lot or batch true Serial number false Manufacturing date on label false Expiration date on label true Donation ID number false Contains natural rubber latex false No natural rubber latex false Sterilization required before use false Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 07640387660140 GoPLF! Posterior Lateral Fusion Device 3100010 2023-12-12 07640387660003 GoPLF! Posterior Lateral Fusion Device 3205535 2022-02-21 07640387660010 GoPLF! Posterior Lateral Fusion Device 3205540 2022-02-21 07640387660027 GoPLF! Posterior Lateral Fusion Device 3205545 2022-02-21 07640387660034 GoPLF! Posterior Lateral Fusion Device 3205550 2022-02-21 07640387660041 GoPLF! Posterior Lateral Fusion Device 3206535 2022-02-21 07640387660058 GoPLF! Posterior Lateral Fusion Device 3206540 2022-02-21 07640387660065 GoPLF! Posterior Lateral Fusion Device 3206545 2023-12-12 07640387660072 GoPLF! Posterior Lateral Fusion Device 3206550 2023-12-12 07640387660089 GoPLF! Posterior Lateral Fusion Device 3206555 2023-12-12 07640387660096 GoPLF! Posterior Lateral Fusion Device 3207535 2023-12-12 07640387660102 GoPLF! Posterior Lateral Fusion Device 3207540 2023-12-12 07640387660119 GoPLF! Posterior Lateral Fusion Device 3207545 2023-12-12 07640387660126 GoPLF! Posterior Lateral Fusion Device 3207550 2023-12-12 07640387660133 GoPLF! Posterior Lateral Fusion Device 3207555 2023-12-12 07640387660157 GoPLF! Posterior Lateral Fusion Device 3200035 2023-12-12 07640387660164 GoPLF! Posterior Lateral Fusion Device 3200040 2023-12-12 07640387660171 GoPLF! Posterior Lateral Fusion Device 3200045 2023-12-12 07640387660188 GoPLF! Posterior Lateral Fusion Device 3200050 2023-12-12 07640387660195 GoPLF! Posterior Lateral Fusion Device 3200055 2023-12-12
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