DUALXS T/PLIF LOCKOUT SCREW SHORT

GUDID B707128400060010

DUALXS T/PLIF LOCKOUT SCREW SHORT

AMPLIFY SURGICAL, INC.

Metallic spinal interbody fusion cage

• Primary Device ID: B707128400060010
• NIH Device Record Key: d2587e90-a3f1-48a1-9916-7cb9ed07fd3a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DUALXS T/PLIF LOCKOUT SCREW SHORT
• Version Model Number: 12840006001
• Company DUNS: 081021000
• Company Name: AMPLIFY SURGICAL, INC.
• 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: 7652675439
• Email: UDI@AMPLIFYSURGICAL.COM
• Phone: 7652675439
• Email: UDI@AMPLIFYSURGICAL.COM
• Phone: 7652675439
• Email: UDI@AMPLIFYSURGICAL.COM
• Phone: 7652675439
• Email: UDI@AMPLIFYSURGICAL.COM
• Phone: 7652675439
• Email: UDI@AMPLIFYSURGICAL.COM
• Phone: 7652675439
• Email: UDI@AMPLIFYSURGICAL.COM
• Phone: 7652675439
• Email: UDI@AMPLIFYSURGICAL.COM
• Phone: 7652675439
• Email: UDI@AMPLIFYSURGICAL.COM
• Phone: 7652675439
• Email: UDI@AMPLIFYSURGICAL.COM
• Phone: 7652675439
• Email: UDI@AMPLIFYSURGICAL.COM
• Phone: 7652675439
• Email: UDI@AMPLIFYSURGICAL.COM
• Phone: 7652675439
• Email: UDI@AMPLIFYSURGICAL.COM
• Phone: 7652675439
• Email: UDI@AMPLIFYSURGICAL.COM
• Phone: 7652675439
• Email: UDI@AMPLIFYSURGICAL.COM
• Phone: 7652675439
• Email: UDI@AMPLIFYSURGICAL.COM
• Phone: 7652675439
• Email: UDI@AMPLIFYSURGICAL.COM
• Phone: 7652675439
• Email: UDI@AMPLIFYSURGICAL.COM
• Phone: 7652675439
• Email: UDI@AMPLIFYSURGICAL.COM

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B707128400060010 [Primary]

FDA Product Code

• MAX: Intervertebral Fusion Device With Bone Graft, Lumbar

Sterilization

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

[B707128400060010]

Moist Heat or Steam Sterilization

[B707128400060010]

Moist Heat or Steam Sterilization

[B707128400060010]

Moist Heat or Steam Sterilization

[B707128400060010]

Moist Heat or Steam Sterilization

[B707128400060010]

Moist Heat or Steam Sterilization

[B707128400060010]

Moist Heat or Steam Sterilization

[B707128400060010]

Moist Heat or Steam Sterilization

[B707128400060010]

Moist Heat or Steam Sterilization

[B707128400060010]

Moist Heat or Steam Sterilization

[B707128400060010]

Moist Heat or Steam Sterilization

[B707128400060010]

Moist Heat or Steam Sterilization

[B707128400060010]

Moist Heat or Steam Sterilization

[B707128400060010]

Moist Heat or Steam Sterilization

[B707128400060010]

Moist Heat or Steam Sterilization

[B707128400060010]

Moist Heat or Steam Sterilization

[B707128400060010]

Moist Heat or Steam Sterilization

[B707128400060010]

Moist Heat or Steam Sterilization

[B707128400060010]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2025-05-21
• Device Publish Date: 2023-01-10

Devices Manufactured by AMPLIFY SURGICAL, INC.

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• B70712535588001US0 - DUALX DUAL PORT CANNULA 30MM: 2025-06-06 30MM US MANUFACTURE
• B70712535588002US0 - DUALX DUAL PORT CANNULA 40MM: 2025-06-06 40MM US MANUFACTURE
• B70712535588003US0 - DUALX DUAL PORT CANNULA 50MM: 2025-06-06 50MM US MANUFACTURE
• B70712535588004US0 - DUALX DUAL PORT CANNULA 60MM: 2025-06-06 60MM US MANUFACTURE
• B70712535588005US0 - DUALX DUAL PORT CANNULA 70MM: 2025-06-06 70MM US MANUFACTURE
• B70712535588006US0 - DUALX DUAL PORTAL CANNULA 80MM: 2025-06-06 80MM US MANUFACTURE
• B70712535588007US0 - DUALX DUAL PORTAL CANNULA 90MM: 2025-06-06 90MM US MANUFACTURE