ProLift Micro

GUDID 00190837141707

Life Spine, Inc.

Metallic spinal interbody fusion cage

• Primary Device ID: 00190837141707
• NIH Device Record Key: a941112e-7d9d-48d5-ae29-136ec0b72711
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ProLift Micro
• Version Model Number: 58-0832-1208M
• 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	00190837141707 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K212520

FDA Product Code

• MAX: Intervertebral Fusion Device With Bone Graft, Lumbar

Sterilization

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

[00190837141707]

Radiation Sterilization

[00190837141707]

Radiation Sterilization

[00190837141707]

Radiation Sterilization

[00190837141707]

Radiation Sterilization

[00190837141707]

Radiation Sterilization

[00190837141707]

Radiation Sterilization

[00190837141707]

Radiation Sterilization

[00190837141707]

Radiation Sterilization

[00190837141707]

Radiation Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-08-03
• Device Publish Date: 2022-07-26

On-Brand Devices [ProLift Micro]

• 00190837141684: 58-0832-0813M
• 00190837141707: 58-0832-1208M
• 00190837141660: 58-0832-0708M
• 00190837141721: 58-0832-1508M