Home GUDID 00841732105157
MATISSE Anterior Cervical Interbody Fusion Cage System
Primary DI 00841732105157
Brand MATISSE Anterior Cervical Interbody Fusion Cage System
Company CTL Medical Corporation
Model 013.4118
Device description MATISSE ACIF Cage, PEEK, W14 x L12, 6Deg., H8mm
Published 2016-03-05
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Single use true
Product Codes# Code, Name table Code Name ODP Intervertebral fusion device with bone graft, cervical
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class ODP Intervertebral Fusion Device With Bone Graft, Cervical Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00841732105157 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 00841732105157 00841732105157 841732105157 0841732105157
GMDN Terms# Term, Definition table Term Definition Polymeric spinal interbody fusion cage A device intended to be implanted into the space of an intervertebral disc that has been partially or totally removed during surgery in order to allow bone fusion between two contiguous vertebral bodies, typically in the treatment of degenerative disc disease (DDD). It is in the form of a hollow, porous, threaded and/or fenestrated cylindrical or geometrical device made of non-bioabsorbable synthetic polymer [e.g., polyetheretherketone (PEEK)] that provides mechanical stability and sufficient space for therapeutic spinal bone fusion to occur; bone graft is typically used to help with osseointegration. Fixation screws and devices associated with implantation may be included with the device.
Device Sizes# Type, Value, Unit table Type Value Unit Device Size Text, specify 0 Height 8 Millimeter Length 12 Millimeter Width 14 Millimeter
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 00841732163447 VALEO C Spacer System 91.002.4001 2023-09-30 00841732163454 VALEO C Spacer System 91.002.4002 2023-09-30 00841732163461 VALEO C Spacer System 91.002.4003 2023-09-30 00841732128231 VALEO VBR 91.009.5651 2023-09-27 00841732128248 VALEO VBR 91.009.5652 2023-09-27 00841732145511 VALEO C+CSC with Lumen Interbody Fusion Device 11.209.1707 2023-09-19 00841732145528 VALEO C+CSC with Lumen Interbody Fusion Device 11.209.1708 2023-09-19 00841732145535 VALEO C+CSC with Lumen Interbody Fusion Device 11.209.1709 2023-09-19 00841732145542 VALEO C+CSC with Lumen Interbody Fusion Device 11.209.1710 2023-09-19 00841732154766 VALEO C+CSC with Lumen Interbody Fusion Device 11.209.1108 2023-09-19 00841732154773 VALEO C+CSC with Lumen Interbody Fusion Device 11.209.1109 2023-09-19 00841732154780 VALEO C+CSC with Lumen Interbody Fusion Device 11.209.1110 2023-09-19 00841732154797 VALEO C+CSC with Lumen Interbody Fusion Device 11.209.1111 2023-09-19 00841732154803 VALEO C+CSC with Lumen Interbody Fusion Device 11.209.1705 2023-09-19 00841732154810 VALEO C+CSC with Lumen Interbody Fusion Device 11.209.1706 2023-09-19 00841732154865 VALEO C+CSC with Lumen Interbody Fusion Device 11.209.1711 2023-09-19 00841732149847 TAURUS Pedicle Screw System 51-1000-001 2023-09-15 00841732149854 TAURUS Pedicle Screw System 51-1000-002 2023-09-15 00841732150614 GENERIC Surgical Instruments 50-1000-004 2023-09-15 00841732150621 TAURUS Pedicle Screw System 51-0000-000 2023-09-15
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