ProLift Pivot

GUDID 00190837202774

Life Spine, Inc.

Metallic spinal interbody fusion cage

• Primary Device ID: 00190837202774
• NIH Device Record Key: 74703e5f-4f5f-4918-89fe-de022682d89c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ProLift Pivot
• Version Model Number: 15-1026-0708
• Company DUNS: 183641617
• Company Name: Life Spine, 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00190837202774 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K243668

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: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-08-29
• Device Publish Date: 2025-08-21

Devices Manufactured by Life Spine, Inc.

• 00190837202774 - ProLift Pivot: 2025-08-29
• 00190837202774 - ProLift Pivot: 2025-08-29
• 00190837171889 - AVATAR Minimally Invasive Spinal System Instruments: 2025-07-15
• 00190837142186 - ProLift: 2025-07-09
• 00190837037499 - ProLift Lateral: 2025-07-02
• 00190837133030 - ARx: 2025-07-02
• 00190837133757 - ARx: 2025-07-02
• 00190837133795 - ARx: 2025-07-02
• 00190837133832 - ARx: 2025-07-02