Home GUDID 00841732140905
RENOIR Posterior Cervical Fixation System
Primary DI 00841732140905
Brand RENOIR Posterior Cervical Fixation System
Company CTL Medical Corporation
Model 012.7074
Device description Rocker Arm, Housing Top
Published 2024-01-04
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Product Codes# Code, Name table Code Name KWP Appliance, Fixation, Spinal Interlaminal MNI ORTHOSIS, SPINAL PEDICLE FIXATION
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class KWP Appliance, Fixation, Spinal Interlaminal Orthopedic 2 MNI Orthosis, Spinal Pedicle Fixation Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00841732140905 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, UPC-A table Source identifier GTIN-14 normalized UPC-A EAN-13 00841732140905 00841732140905 841732140905 0841732140905
GMDN Terms# Term, Definition table Term Definition Bone-screw internal spinal fixation system, non-sterile An assembly of non-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. Non-sterile disposable devices associated with implantation may be included.
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 080138504 Device count 1 Lot or batch true Manufacturing date on label true Sterilization required before use true Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 00841732155671 VALEO II PL OL Interbody Fusion System 12.301.1012 2023-09-27 00841732155688 VALEO II PL OL Interbody Fusion System 12.301.1013 2023-09-27 00841732155695 VALEO II PL OL Interbody Fusion System 12.301.1015 2023-09-27 00841732155701 VALEO II PL OL Interbody Fusion System 12.301.1014 2023-09-27 00841732155718 VALEO II PL OL Interbody Fusion System 12.301.1016 2023-09-27 00841732155725 VALEO II PL OL Interbody Fusion System 12.301.1508 2023-09-27 00841732155732 VALEO II PL OL Interbody Fusion System 12.301.1509 2023-09-27 00841732155749 VALEO II PL OL Interbody Fusion System 12.301.1510 2023-09-27 00841732155756 VALEO II PL OL Interbody Fusion System 12.301.1511 2023-09-27 00841732155763 VALEO II PL OL Interbody Fusion System 12.301.1512 2023-09-27 00841732155770 VALEO II PL OL Interbody Fusion System 12.301.1513 2023-09-27 00841732155787 VALEO II PL OL Interbody Fusion System 12.301.1514 2023-09-27 00841732155794 VALEO II PL OL Interbody Fusion System 12.301.1515 2023-09-27 00841732155800 VALEO II PL OL Interbody Fusion System 12.301.1516 2023-09-27 00841732156135 VALEO II PL OL Interbody Fusion System 12.301.2007 2023-09-27 00841732156142 VALEO II PL OL Interbody Fusion System 12.301.2008 2023-09-27 00841732156159 VALEO II PL OL Interbody Fusion System 12.301.2009 2023-09-27 00841732156166 VALEO II PL OL Interbody Fusion System 12.301.2010 2023-09-27 00841732156173 VALEO II PL OL Interbody Fusion System 12.301.2011 2023-09-27 00841732156180 VALEO II PL OL Interbody Fusion System 12.301.2012 2023-09-27
Other Devices Sharing Product Codes#