DUALX TLIF TRIAL 13-16MM

GUDID B70712535200007A0

DUALX TLIF TRIAL 13-16MM

AMPLIFY SURGICAL, INC.

Spinal implant trial Spinal implant trial

• Primary Device ID: B70712535200007A0
• NIH Device Record Key: c92b30a5-29a5-4ce6-a477-1fa304cbb00a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DUALX TLIF TRIAL 13-16MM
• Version Model Number: 12535200007A0
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• 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: 949-220-1286
• Email: admin@innovasiveinc.com
• Phone: 949-220-1286
• Email: admin@innovasiveinc.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B70712535200007A0 [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: true
• Device Is Sterile: false

[B70712535200007A0]

Moist Heat or Steam Sterilization

[B70712535200007A0]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-05-13
• Device Publish Date: 2019-01-08

On-Brand Devices [DUALX TLIF TRIAL 13-16MM]

• B70712535200007A0: DUALX TLIF TRIAL 13-16MM
• B707125352000070: DUALX TLIF TRIAL 13-16MM Rev D
• B707125354000080: DUALX TLIF TRIAL 13-16MM