TrellOss®

GUDID 00840067208588

TrellOss-C 16Dx18Wx8H 10°

NEXXT SPINE, LLC

Metallic spinal interbody fusion cage

• Primary Device ID: 00840067208588
• NIH Device Record Key: 69222d6e-07ce-462d-9f9d-2758e1e43546
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TrellOss®
• Version Model Number: 110N1608
• 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: 16 Millimeter
• Width: 18 Millimeter
• Height: 8 Millimeter
• Angle: 10 degree
• Depth: 16 Millimeter
• Width: 18 Millimeter
• Height: 8 Millimeter
• Angle: 10 degree
• Depth: 16 Millimeter
• Width: 18 Millimeter
• Height: 8 Millimeter
• Angle: 10 degree
• Depth: 16 Millimeter
• Width: 18 Millimeter
• Height: 8 Millimeter
• Angle: 10 degree
• Depth: 16 Millimeter
• Width: 18 Millimeter
• Height: 8 Millimeter
• Angle: 10 degree
• Depth: 16 Millimeter
• Width: 18 Millimeter
• Height: 8 Millimeter
• Angle: 10 degree
• Depth: 16 Millimeter
• Width: 18 Millimeter
• Height: 8 Millimeter
• Angle: 10 degree
• Depth: 16 Millimeter
• Width: 18 Millimeter
• Height: 8 Millimeter
• Angle: 10 degree
• Depth: 16 Millimeter
• Width: 18 Millimeter
• Height: 8 Millimeter
• Angle: 10 degree
• Depth: 16 Millimeter
• Width: 18 Millimeter
• Height: 8 Millimeter
• Angle: 10 degree
• Depth: 16 Millimeter
• Width: 18 Millimeter
• Height: 8 Millimeter
• Angle: 10 degree
• Depth: 16 Millimeter
• Width: 18 Millimeter
• Height: 8 Millimeter
• Angle: 10 degree

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840067208588 [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: 2025-08-06
• Device Publish Date: 2025-07-29

On-Brand Devices [TrellOss®]

• 00840067208625: TrellOss-C 16Dx18Wx12H 10°
• 00840067208618: TrellOss-C 16Dx18Wx11H 10°
• 00840067208601: TrellOss-C 16Dx18Wx10H 10°
• 00840067208595: TrellOss-C 16Dx18Wx9H 10°
• 00840067208588: TrellOss-C 16Dx18Wx8H 10°
• 00840067208571: TrellOss-C 16Dx18Wx7H 10°
• 00840067208564: TrellOss-C 16Dx18Wx6H 10°
• 00840067208557: TrellOss-C 14Dx16Wx12H 10°
• 00840067208540: TrellOss-C 14Dx16Wx11H 10°
• 00840067208533: TrellOss-C 14Dx16Wx10H 10°
• 00840067208526: TrellOss-C 14Dx16Wx9H 10°
• 00840067208519: TrellOss-C 14Dx16Wx8H 10°
• 00840067208502: TrellOss-C 14Dx16Wx7H 10°
• 00840067208496: TrellOss-C 14Dx16Wx6H 10°
• 00840067208489: TrellOss-C 12Dx14Wx12H 10°
• 00840067208472: TrellOss-C 12Dx14Wx11H 10°
• 00840067208465: TrellOss-C 12Dx14Wx10H 10°
• 00840067208458: TrellOss-C 12Dx14Wx9H 10°
• 00840067208441: TrellOss-C 12Dx14Wx8H 10°
• 00840067208434: TrellOss-C 12Dx14Wx7H 10°
• 00840067208427: TrellOss-C 12Dx14Wx6H 10°