AVANT 6400-02N

GUDID 00193082161711

AVANT Polyaxial Screwdriver, Navigted

SPINECRAFT, LLC

Stereotactic surgery system probe, reusable

• Primary Device ID: 00193082161711
• NIH Device Record Key: 7708fd49-9d9c-40d2-ad14-17e912bb4bf6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AVANT
• Version Model Number: 6400-02N
• Catalog Number: 6400-02N
• Company DUNS: 783908713
• Company Name: SPINECRAFT, LLC
• 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: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(630)920-7300
• Email: info@spinecraft.com
• Phone: +1(630)920-7300
• Email: info@spinecraft.com
• Phone: +1(630)920-7300
• Email: info@spinecraft.com
• Phone: +1(630)920-7300
• Email: info@spinecraft.com
• Phone: +1(630)920-7300
• Email: info@spinecraft.com
• Phone: +1(630)920-7300
• Email: info@spinecraft.com
• Phone: +1(630)920-7300
• Email: info@spinecraft.com
• Phone: +1(630)920-7300
• Email: info@spinecraft.com
• Phone: +1(630)920-7300
• Email: info@spinecraft.com
• Phone: +1(630)920-7300
• Email: info@spinecraft.com
• Phone: +1(630)920-7300
• Email: info@spinecraft.com
• Phone: +1(630)920-7300
• Email: info@spinecraft.com
• Phone: +1(630)920-7300
• Email: info@spinecraft.com
• Phone: +1(630)920-7300
• Email: info@spinecraft.com
• Phone: +1(630)920-7300
• Email: info@spinecraft.com
• Phone: +1(630)920-7300
• Email: info@spinecraft.com
• Phone: +1(630)920-7300
• Email: info@spinecraft.com
• Phone: +1(630)920-7300
• Email: info@spinecraft.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00193082161711 [Primary]

FDA Product Code

• OLO: Orthopedic stereotaxic instrument

Sterilization

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

[00193082161711]

Moist Heat or Steam Sterilization

[00193082161711]

Moist Heat or Steam Sterilization

[00193082161711]

Moist Heat or Steam Sterilization

[00193082161711]

Moist Heat or Steam Sterilization

[00193082161711]

Moist Heat or Steam Sterilization

[00193082161711]

Moist Heat or Steam Sterilization

[00193082161711]

Moist Heat or Steam Sterilization

[00193082161711]

Moist Heat or Steam Sterilization

[00193082161711]

Moist Heat or Steam Sterilization

[00193082161711]

Moist Heat or Steam Sterilization

[00193082161711]

Moist Heat or Steam Sterilization

[00193082161711]

Moist Heat or Steam Sterilization

[00193082161711]

Moist Heat or Steam Sterilization

[00193082161711]

Moist Heat or Steam Sterilization

[00193082161711]

Moist Heat or Steam Sterilization

[00193082161711]

Moist Heat or Steam Sterilization

[00193082161711]

Moist Heat or Steam Sterilization

[00193082161711]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-01-30
• Device Publish Date: 2024-01-22

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• 00193082163180 - ORIO: 2025-02-07 PLIF Disc Shaver, 8mm
• 00193082163197 - ORIO: 2025-02-07 PLIF Disc Shaver, 10mm
• 00193082163203 - ORIO: 2025-02-07 PLIF Disc Shaver, 12mm
• 00193082155888 - ASTRA Spine System: 2024-11-18 ASTRA Table Top Rod Cutter
• 00193082155895 - APEX Spine System: 2024-11-18 In-situ Coronal Rod Bender, Left (Dia. 6.2mm Rod Compatible)
• 00193082155901 - APEX Spine System: 2024-11-18 In-situ Coronal Rod Bender, Right (Dia 6.2mm Rod Compatible)