NeoSpan® T05 S0003

GUDID 00810021869681

NeoSpan Compression Implant System,Implant Screw Kit,Sterile

IN2BONES USA, LLC

General internal orthopaedic fixation system implantation kit

• Primary Device ID: 00810021869681
• NIH Device Record Key: 9e14ee68-cc02-4907-82d2-4b2d39399d0c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NeoSpan®
• Version Model Number: T05 S0003
• Catalog Number: T05 S0003
• Company DUNS: 079700711
• Company Name: IN2BONES USA, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: true
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810021869681 [Primary]

FDA Product Code

• LXH: Orthopedic manual surgical instrument

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2025-01-03
• Device Publish Date: 2024-12-10

On-Brand Devices [NeoSpan®]

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• 00810021869650: NeoSpan Implant +2H w/ Instruments, Sterile, Size, 18mm x 2
• 00810021869643: NeoSpan Implant +2H w/ Instruments, Sterile, Size, 18mm x 2
• 00810021869636: NeoSpan Implant +3H w/ Instruments, Sterile, Size, 18mm x 14
• 00810021869629: NeoSpan Implant +2H w/ Instruments, Sterile, Size, 18mm x 1
• 00810021869612: NeoSpan Implant +1H w/ Instruments, Sterile, Size, 18mm x 1
• 00810021869605: NeoSpan Implant, T-shape +2H w/ Instruments, Sterile
• 00810021869599: NeoSpan Implant, T-shape +1H w/ Instruments, Sterile
• 00810021869582: NeoSpan Implant, T-shape w/ Instruments, Sterile
• 00810021869575: NeoSpan Implant w/ Instruments, Sterile, Size, 18mm x 14mm
• 00810021869568: NeoSpan Implant w/ Instruments, Sterile, Size, 25mm x 22mm
• 00810021869551: NeoSpan Implant w/ Instruments, Sterile, Size, 20mm x 20mm
• 00810021869544: NeoSpan Implant w/ Instruments, Sterile, Size, 18mm x 18mm
• 00810021869537: NeoSpan Implant w/ Instruments, Sterile, Size 18mm x 16mm
• 00810021869681: NeoSpan Compression Implant System,Implant Screw Kit,Sterile
• 00810021869674: NeoSpan Compression Implant System,Implant Trial Kit,Sterile