Brickyard ALIF

GUDID 00843210177946

42mm x 30mm, 20°, 17mm Trial

Altus Spine, LLC

Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial

• Primary Device ID: 00843210177946
• NIH Device Record Key: d9a4f136-a1f9-47dc-b6be-342aced878e7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Brickyard ALIF
• Version Model Number: 1020-42302017
• Company DUNS: 078331322
• Company Name: Altus 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: true
• Expiration Date: false
• 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(610)355-4156
• Email: Info@altus-spine.com
• Phone: +1(610)355-4156
• Email: Info@altus-spine.com
• Phone: +1(610)355-4156
• Email: Info@altus-spine.com
• Phone: +1(610)355-4156
• Email: Info@altus-spine.com
• Phone: +1(610)355-4156
• Email: Info@altus-spine.com
• Phone: +1(610)355-4156
• Email: Info@altus-spine.com
• Phone: +1(610)355-4156
• Email: Info@altus-spine.com
• Phone: +1(610)355-4156
• Email: Info@altus-spine.com
• Phone: +1(610)355-4156
• Email: Info@altus-spine.com
• Phone: +1(610)355-4156
• Email: Info@altus-spine.com
• Phone: +1(610)355-4156
• Email: Info@altus-spine.com

Device Dimensions

• Angle: 20 degree
• Height: 17 Millimeter
• Angle: 20 degree
• Height: 17 Millimeter
• Angle: 20 degree
• Height: 17 Millimeter
• Angle: 20 degree
• Height: 17 Millimeter
• Angle: 20 degree
• Height: 17 Millimeter
• Angle: 20 degree
• Height: 17 Millimeter
• Angle: 20 degree
• Height: 17 Millimeter
• Angle: 20 degree
• Height: 17 Millimeter
• Angle: 20 degree
• Height: 17 Millimeter
• Angle: 20 degree
• Height: 17 Millimeter
• Angle: 20 degree
• Height: 17 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00843210177946 [Primary]

FDA Product Code

• MAX: Intervertebral fusion device with bone graft, lumbar

Sterilization

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

[00843210177946]

Moist Heat or Steam Sterilization

[00843210177946]

Moist Heat or Steam Sterilization

[00843210177946]

Moist Heat or Steam Sterilization

[00843210177946]

Moist Heat or Steam Sterilization

[00843210177946]

Moist Heat or Steam Sterilization

[00843210177946]

Moist Heat or Steam Sterilization

[00843210177946]

Moist Heat or Steam Sterilization

[00843210177946]

Moist Heat or Steam Sterilization

[00843210177946]

Moist Heat or Steam Sterilization

[00843210177946]

Moist Heat or Steam Sterilization

[00843210177946]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-05-02
• Device Publish Date: 2024-04-24

Devices Manufactured by Altus Spine, LLC

• 00843210167916 - Sochi: 2024-07-04 Self Tapping Occipital Screw, 4.5mm x 17mm
• 00843210167923 - Sochi: 2024-07-04 Self Tapping Occipital Screw, 4.5mm x 18mm
• 00843210167930 - Sochi: 2024-07-04 Self Tapping Occipital Screw, 4.5mm x 20mm
• 00843210167947 - Sochi: 2024-07-04 Self Tapping Occipital Screw, 4.5mm x 22mm
• 00843210167954 - Sochi: 2024-07-04 Self Tapping Occipital Screw, 4.5mm x 24mm
• 00843210167961 - Sochi: 2024-07-04 Self Tapping Occipital Screw, 4.5mm x 26mm
• 00843210167978 - Sochi: 2024-07-04 Self Tapping Occipital Screw, 4.5mm x 28mm
• 00843210177946 - Brickyard ALIF: 2024-05-0242mm x 30mm, 20°, 17mm Trial
• 00843210177946 - Brickyard ALIF: 2024-05-02 42mm x 30mm, 20°, 17mm Trial