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

Devices Manufactured by SPINECRAFT, LLC

• 00193082151972 - APEX Spine System: 2024-08-16 APEX Ti Rod Dia. 5.5 x 110mm, Lordosed
• 00193082151989 - APEX Spine System: 2024-08-16 APEX Ti Rod Dia. 5.5 x 120mm, Lordosed
• 00193082151996 - APEX Spine System: 2024-08-16 APEX Ti Rod Dia. 5.5 x 130mm, Lordosed
• 00193082152009 - APEX Spine System: 2024-08-16 APEX Ti Rod Dia. 5.5 x 200mm, Lordosed
• 00193082152016 - APEX Spine System: 2024-08-16 APEX Ti Rod Dia. 6 x 110mm, Lordosed
• 00193082152023 - APEX Spine System: 2024-08-16 APEX Ti Rod Dia. 6 x 120mm, Lordosed
• 00193082152030 - APEX Spine System: 2024-08-16 APEX Ti Rod Dia. 6 x 130mm, Lordosed
• 00193082152047 - APEX Spine System: 2024-08-16 APEX Ti Rod Dia. 6 x 200mm, Lordosed