TrellOss®-C

GUDID 00840067209653

TrellOss-C 12Dx14Wx7H 15°

NEXXT SPINE, LLC

Metallic spinal interbody fusion cage

• Primary Device ID: 00840067209653
• NIH Device Record Key: a677e113-0eb6-4ca7-b737-602f9364bf7e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TrellOss®-C
• Version Model Number: 111N1207
• Company DUNS: 003489810
• Company Name: NEXXT SPINE, 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: false
• Device Combination Product: false
• Single Use: true
• 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: 317-436-7801
• Email: Support@nexxtspine.com
• Phone: 317-436-7801
• Email: Support@nexxtspine.com
• Phone: 317-436-7801
• Email: Support@nexxtspine.com
• Phone: 317-436-7801
• Email: Support@nexxtspine.com
• Phone: 317-436-7801
• Email: Support@nexxtspine.com
• Phone: 317-436-7801
• Email: Support@nexxtspine.com
• Phone: 317-436-7801
• Email: Support@nexxtspine.com
• Phone: 317-436-7801
• Email: Support@nexxtspine.com
• Phone: 317-436-7801
• Email: Support@nexxtspine.com
• Phone: 317-436-7801
• Email: Support@nexxtspine.com
• Phone: 317-436-7801
• Email: Support@nexxtspine.com
• Phone: 317-436-7801
• Email: Support@nexxtspine.com

Device Dimensions

• Depth: 12 Millimeter
• Width: 14 Millimeter
• Height: 7 Millimeter
• Angle: 15 degree
• Depth: 12 Millimeter
• Width: 14 Millimeter
• Height: 7 Millimeter
• Angle: 15 degree
• Depth: 12 Millimeter
• Width: 14 Millimeter
• Height: 7 Millimeter
• Angle: 15 degree
• Depth: 12 Millimeter
• Width: 14 Millimeter
• Height: 7 Millimeter
• Angle: 15 degree
• Depth: 12 Millimeter
• Width: 14 Millimeter
• Height: 7 Millimeter
• Angle: 15 degree
• Depth: 12 Millimeter
• Width: 14 Millimeter
• Height: 7 Millimeter
• Angle: 15 degree
• Depth: 12 Millimeter
• Width: 14 Millimeter
• Height: 7 Millimeter
• Angle: 15 degree
• Depth: 12 Millimeter
• Width: 14 Millimeter
• Height: 7 Millimeter
• Angle: 15 degree
• Depth: 12 Millimeter
• Width: 14 Millimeter
• Height: 7 Millimeter
• Angle: 15 degree
• Depth: 12 Millimeter
• Width: 14 Millimeter
• Height: 7 Millimeter
• Angle: 15 degree
• Depth: 12 Millimeter
• Width: 14 Millimeter
• Height: 7 Millimeter
• Angle: 15 degree
• Depth: 12 Millimeter
• Width: 14 Millimeter
• Height: 7 Millimeter
• Angle: 15 degree

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840067209653 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K171140

FDA Product Code

• MQP: Spinal Vertebral Body Replacement Device

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-12-17
• Device Publish Date: 2025-12-09

On-Brand Devices [TrellOss®-C]

• 00840067209806: TrellOss-C 16Dx18Wx12H 15°
• 00840067209790: TrellOss-C 16Dx18Wx11H 15°
• 00840067209783: TrellOss-C 16Dx18Wx10H 15°
• 00840067209776: TrellOss-C 16Dx18Wx9H 15°
• 00840067209769: TrellOss-C 16Dx18Wx8H 15°
• 00840067209752: TrellOss-C 14Dx16Wx12H 15°
• 00840067209745: TrellOss-C 14Dx16Wx11H 15°
• 00840067209738: TrellOss-C 14Dx16Wx10H 15°
• 00840067209721: TrellOss-C 14Dx16Wx9H 15°
• 00840067209714: TrellOss-C 14Dx16Wx8H 15°
• 00840067209707: TrellOss-C 12Dx14Wx12H 15°
• 00840067209691: TrellOss-C 12Dx14Wx11H 15°
• 00840067209684: TrellOss-C 12Dx14Wx10H 15°
• 00840067209677: TrellOss-C 12Dx14Wx9H 15°
• 00840067209660: TrellOss-C 12Dx14Wx8H 15°
• 00840067209653: TrellOss-C 12Dx14Wx7H 15°