icotec Cervical Cage, Lordotic, 6 mm x 16 mm 12-40-0616

GUDID 07640140430621

icotec Cervical Cage, Lordotic, 6 mm x 16 mm

icotec AG

Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage

• Primary Device ID: 07640140430621
• NIH Device Record Key: 88d8198f-3baa-4864-a11a-e497c17e8882
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: icotec Cervical Cage, Lordotic, 6 mm x 16 mm
• Version Model Number: 12-40-0616
• Catalog Number: 12-40-0616
• Company DUNS: 480789465
• Company Name: icotec AG
• 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: +41717570000
• Email: info@icotec.ch
• Phone: +41717570000
• Email: info@icotec.ch
• Phone: +41717570000
• Email: info@icotec.ch
• Phone: +41717570000
• Email: info@icotec.ch
• Phone: +41717570000
• Email: info@icotec.ch
• Phone: +41717570000
• Email: info@icotec.ch
• Phone: +41717570000
• Email: info@icotec.ch
• Phone: +41717570000
• Email: info@icotec.ch
• Phone: +41717570000
• Email: info@icotec.ch
• Phone: +41717570000
• Email: info@icotec.ch
• Phone: +41717570000
• Email: info@icotec.ch
• Phone: +41717570000
• Email: info@icotec.ch
• Phone: +41717570000
• Email: info@icotec.ch
• Phone: +41717570000
• Email: info@icotec.ch
• Phone: +41717570000
• Email: info@icotec.ch

Device Identifiers

Device Issuing Agency	Device ID
GS1	07640140430621 [Primary]

FDA Product Code

• ODP: Intervertebral Fusion Device With Bone Graft, Cervical

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: 2022-09-06
• Device Publish Date: 2022-08-29

Devices Manufactured by icotec AG

• 07640164846675 - VADER Pedicle System MIS, Rod, Carbon/PEEK, Straight, Ø 6.0 r000 x 30 mm: 2024-04-04 VADER Pedicle System MIS, Rod, Carbon/PEEK, Straight, Ø 6.0 r000 x 30 mm
• 07640164846804 - VADER Pedicle System MIS, Rod, Carbon/PEEK, Curved, Ø 6.0 r120 x 30 mm: 2024-04-04 VADER Pedicle System MIS, Rod, Carbon/PEEK, Curved, Ø 6.0 r120 x 30 mm
• 07640164846880 - VADER Pedicle System MIS, Rod, Carbon/PEEK, Curved, Ø 6.0 r450 x 30 mm: 2024-04-04 VADER Pedicle System MIS, Rod, Carbon/PEEK, Curved, Ø 6.0 r450 x 30 mm
• 07640164848785 - icotec Pedicle System 6.0, Screw, Ti, Polyaxial, Ø 8.5 x 35 mm: 2024-04-04 icotec Pedicle System 6.0, Screw, Ti, Polyaxial, Ø 8.5 x 35 mm
• 07640164848792 - icotec Pedicle System 6.0, Screw, Ti, Polyaxial, Ø 8.5 x 40 mm: 2024-04-04 icotec Pedicle System 6.0, Screw, Ti, Polyaxial, Ø 8.5 x 40 mm
• 07640164848808 - icotec Pedicle System 6.0, Screw, Ti, Polyaxial, Ø 8.5 x 45 mm: 2024-04-04 icotec Pedicle System 6.0, Screw, Ti, Polyaxial, Ø 8.5 x 45 mm
• 07640164848815 - icotec Pedicle System 6.0, Screw, Ti, Polyaxial, Ø 8.5 x 50 mm: 2024-04-04 icotec Pedicle System 6.0, Screw, Ti, Polyaxial, Ø 8.5 x 50 mm
• 07640164848822 - icotec Pedicle System 6.0, Screw, Ti, Polyaxial, Ø 8.5 x 55 mm: 2024-04-04 icotec Pedicle System 6.0, Screw, Ti, Polyaxial, Ø 8.5 x 55 mm