Allograft Wedge 174-001

GUDID 00190837032081

Life Spine, Inc.

Spinal fixation plate, non-bioabsorbable

• Primary Device ID: 00190837032081
• NIH Device Record Key: e3cf0eb7-5311-4a47-adba-7041c7c83b77
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Allograft Wedge
• Version Model Number: 174-001
• Catalog Number: 174-001
• 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: 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	00190837032081 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K181717

FDA Product Code

• NQW: ORTHOSIS, SPINE, PLATE, LAMINOPLASTY, METAL

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: 2019-11-15
• Device Publish Date: 2019-11-07

On-Brand Devices [Allograft Wedge]

• 00190837085629: 2019-0075
• 00190837032081: 174-001