ProLift Expandable Interbody, 10mm x 28mm, Small 12 degree

GUDID 00190837018986

Life Spine, Inc.

Metallic spinal fusion cage, non-sterile

• Primary Device ID: 00190837018986
• NIH Device Record Key: 0e257b4c-2843-4edd-98cc-24bc33af57a2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ProLift Expandable Interbody, 10mm x 28mm, Small 12 degree
• Version Model Number: 58-1028-1208
• Company DUNS: 183641617
• Company Name: Life Spine, Inc.
• Device Count: 1
• DM Exempt: true
• 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: false
• 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	00190837018986 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K153400

FDA Product Code

• MAX: Intervertebral Fusion Device With Bone Graft, Lumbar

Sterilization

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

[00190837018986]

Radiation Sterilization

[00190837018986]

Radiation Sterilization

[00190837018986]

Radiation Sterilization

[00190837018986]

Radiation Sterilization

[00190837018986]

Radiation Sterilization

[00190837018986]

Radiation Sterilization

[00190837018986]

Radiation Sterilization

[00190837018986]

Radiation Sterilization

[00190837018986]

Radiation Sterilization

[00190837018986]

Radiation Sterilization

[00190837018986]

Radiation Sterilization

[00190837018986]

Radiation Sterilization

[00190837018986]

Radiation Sterilization

[00190837018986]

Radiation Sterilization

[00190837018986]

Radiation Sterilization

[00190837018986]

Radiation Sterilization

[00190837018986]

Radiation Sterilization

[00190837018986]

Radiation Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2017-06-08

Devices Manufactured by Life Spine, Inc.

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• 00190837175191 - ARx SAI: 2024-12-12
• 00190837175238 - ARx SAI: 2024-12-12
• 00190837175382 - ARx SAI: 2024-12-12
• 00190837153410 - TruLift Lateral: 2024-10-25
• 00190837142209 - ProLift: 2024-10-18
• 00190837142278 - ProLift: 2024-10-18