KIT DUALX PLIF 8 DEG x 13-16MM

GUDID B707128230000090

PLIF IMPLANT Lordosis & Heights: 8° x 13-16mm Collapsed Width (mm): 12.32 Expanded Width (mm): 21.1 Collapsed Height (mm): 13.21 Expanded Height (mm): 16.5 Collapsed Length (mm): 39.69 Expanded Length (mm): 33.4 PLIF SCREW

AMPLIFY SURGICAL, INC.

Metallic spinal interbody fusion cage

• Primary Device ID: B707128230000090
• NIH Device Record Key: 8a7c92b8-eca5-4e80-a6a8-22e958409c5f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: KIT DUALX PLIF 8 DEG x 13-16MM
• Version Model Number: 12823000009
• 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B707128230000090 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K181397

FDA Product Code

• MAX: Intervertebral Fusion Device With Bone Graft, Lumbar

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-02-24
• Device Publish Date: 2019-05-10

Devices Manufactured by AMPLIFY SURGICAL, INC.

• B707125342180 - DUALX ACME PIN: 2024-09-11 DUALX ACME PIN
• B707128440050 - DualXS Implant Retainer Shaft: 2024-09-11 DUALXS IMPLANT RETAINER SHAFT
• B707128450000 - DualXS Inserter Outer Shaft: 2024-09-11 DUALXS INSERTER OUTER SHAFT ASSEMBLY
• B707128450010 - DualXS Fixed ACME Drawbar: 2024-09-11 DualXS Fixed ACME Drawbar
• B707128450020 - DualXS Inserter Handle Acme: 2024-09-11 DualXS Inserter Handle Acme
• B707129410010040 - DUALXS T/PLIF 8 DEG x 7-9MM: 2024-06-28 Lordosis & Heights: 8° x 7-9mm Collapsed Width (mm): 10 Expanded Width (mm): 20 Collapsed Height (mm): 7 Expanded Height (mm):
• B707129410010050 - DUALXS T/PLIF 12 DEG x 7-10MM: 2024-06-28 Lordosis & Heights: 8° x 7-10mm Collapsed Width (mm): 12 Expanded Width (mm): 20 Collapsed Height (mm): 7 Expanded Height (mm):
• B707129410010120 - DUALXS T/PLIF 15 DEG x 8-11MM: 2024-06-28 Lordosis & Heights: 15° x 8-11mm Collapsed Width (mm): 10 Expanded Width (mm): 20 Collapsed Height (mm): 8 Expanded Height (mm)