Nautilus Non-Cannulated Iliac 485-100-5

GUDID 00190837031343

Life Spine, Inc.

Bone-screw internal spinal fixation system, non-sterile

• Primary Device ID: 00190837031343
• NIH Device Record Key: 322bb220-70d7-4ea8-87d7-4506e20e997d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Nautilus Non-Cannulated Iliac
• Version Model Number: 485-100-5
• Catalog Number: 485-100-5
• 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	00190837031343 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K111953

FDA Product Code

• NKB: Thoracolumbosacral pedicle screw system

Sterilization

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

[00190837031343]

Moist Heat or Steam Sterilization

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 [Nautilus Non-Cannulated Iliac]

• 00190837031367: 485-110-5
• 00190837031350: 485-105-5
• 00190837031343: 485-100-5
• 00190837031336: 485-95-5
• 00190837031329: 475-110-5
• 00190837031312: 475-105-5
• 00190837031305: 475-100-5
• 00190837031299: 475-95-5