Home GUDID 00841132100226
Response Spine 5.5/6.0 System
Primary DI 00841132100226
Brand Response Spine 5.5/6.0 System
Company ORTHOPEDIATRICS CORP.
Model 00-1300-0545
Catalog number 00-1300-0545
Device description 5.5/6.0 UNIAXIAL PEDICLE SCREW 5.0MM X 45MM
Published 2015-06-30
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
Single use true
Product Codes# Code, Name table Code Name KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL MNH Orthosis, spondylolisthesis spinal fixation MNI ORTHOSIS, SPINAL PEDICLE FIXATION NKB Orthosis, spinal pedicle fixation, for degenerative disc disease OSH Pedicle screw spinal system, adolescent idiopathic scoliosis
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class KWP Appliance, Fixation, Spinal Interlaminal Orthopedic 2 MNH Orthosis, Spondylolisthesis Spinal Fixation Orthopedic 2 MNI Orthosis, Spinal Pedicle Fixation Orthopedic 2 NKB Thoracolumbosacral Pedicle Screw System Orthopedic 2 OSH Pedicle Screw Spinal System, Adolescent Idiopathic Scoliosis Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00841132100226 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 00841132100226 00841132100226 841132100226 0841132100226
GMDN Terms# Term, Definition table Term Definition Trans-facet-screw internal spinal fixation system, sterile A sterile device assembly that consists of rods, plates, and facet fixation screws where the screws are inserted bilaterally through and across the facet joint (spinal joint), i.e., trans-facet, at a single or multiple levels to stabilize and fuse vertebrae with compression in the treatment of various spinal conditions.
Regulatory Flags# DUNS number 796416191 Device count 1 DM exempt true Lot or batch true Manufacturing date on label true Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 00841132125014 General Instrument 01-1003-3001 01-1003-3001 2016-09-25 00841132125021 General Instrument 01-1003-3002 01-1003-3002 2016-09-25 00841132125038 General Instrument 01-1003-3003 01-1003-3003 2016-09-25 00841132124277 ACL 01-1008-2530 01-1008-2530 2021-07-06 00841132122112 OrthoPediatrics ACL Reconstruction System 10-1008-1060 10-1008-1060 2015-09-18 00841132122129 OrthoPediatrics ACL Reconstruction System 10-1008-1065 10-1008-1065 2015-09-18 00841132122136 OrthoPediatrics ACL Reconstruction System 10-1008-1070 10-1008-1070 2015-09-18 00841132122143 OrthoPediatrics ACL Reconstruction System 10-1008-1075 10-1008-1075 2015-09-18 00841132122150 OrthoPediatrics ACL Reconstruction System 10-1008-1080 10-1008-1080 2015-09-18 00841132122167 OrthoPediatrics ACL Reconstruction System 10-1008-1085 10-1008-1085 2015-09-18 00841132122174 OrthoPediatrics ACL Reconstruction System 10-1008-1090 10-1008-1090 2015-09-18 00841132122181 OrthoPediatrics ACL Reconstruction System 10-1008-1100 10-1008-1100 2015-09-18 00841132122198 OrthoPediatrics ACL Reconstruction System 10-1008-4060 10-1008-4060 2015-09-18 00841132122204 OrthoPediatrics ACL Reconstruction System 10-1008-4065 10-1008-4065 2015-09-18 00841132122211 OrthoPediatrics ACL Reconstruction System 10-1008-4070 10-1008-4070 2015-09-18 00841132122228 OrthoPediatrics ACL Reconstruction System 10-1008-4075 10-1008-4075 2015-09-18 00841132122235 OrthoPediatrics ACL Reconstruction System 10-1008-4080 10-1008-4080 2015-09-18 00841132122242 OrthoPediatrics ACL Reconstruction System 10-1008-4085 10-1008-4085 2015-09-18 00841132126219 General Instrument 01-1008-0007 01-1008-0007 2016-09-25 00841132126226 General Instrument 01-1008-0010 01-1008-0010 2016-09-25
Other Devices Sharing Product Codes#