Simpact Instrument 2019-0071

GUDID 00190837079789

Triangular Pin Offset Guide, 16-16-18

Life Spine, Inc.

Bone-screw internal spinal fixation system, non-sterile

• Primary Device ID: 00190837079789
• NIH Device Record Key: f5b08900-d7d5-493c-994c-e148f48847f8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Simpact Instrument
• Version Model Number: 2019-0071
• Catalog Number: 2019-0071
• 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: false
• 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	00190837079789 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K180749

FDA Product Code

• OUR: Sacroiliac joint fixation

Sterilization

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

[00190837079789]

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

Devices Manufactured by Life Spine, Inc.

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• 00190837175177 - ARx SAI: 2024-12-12
• 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