Distraction Screw Pre-Drill 7331-40

GUDID 00840199515769

Anterior Lumbar Distraction Screw Pre-Drill 4.5mm

KOROS U.S.A., INC.

Surgical drill guide, reusable

• Primary Device ID: 00840199515769
• NIH Device Record Key: eea37cc1-2d64-4f68-903e-f4aa777a16be
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Distraction Screw Pre-Drill
• Version Model Number: 7331-40
• Catalog Number: 7331-40
• Company DUNS: 007928633
• Company Name: KOROS U.S.A., INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• 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

Customer Support Contacts

• Phone: 1-805-529-0825
• Email: customerservice@korosUSA.com
• Phone: 1-805-529-0825
• Email: customerservice@korosUSA.com
• Phone: 1-805-529-0825
• Email: customerservice@korosUSA.com
• Phone: 1-805-529-0825
• Email: customerservice@korosUSA.com
• Phone: 1-805-529-0825
• Email: customerservice@korosUSA.com
• Phone: 1-805-529-0825
• Email: customerservice@korosUSA.com
• Phone: 1-805-529-0825
• Email: customerservice@korosUSA.com
• Phone: 1-805-529-0825
• Email: customerservice@korosUSA.com
• Phone: 1-805-529-0825
• Email: customerservice@korosUSA.com
• Phone: 1-805-529-0825
• Email: customerservice@korosUSA.com
• Phone: 1-805-529-0825
• Email: customerservice@korosUSA.com
• Phone: 1-805-529-0825
• Email: customerservice@korosUSA.com
• Phone: 1-805-529-0825
• Email: customerservice@korosUSA.com
• Phone: 1-805-529-0825
• Email: customerservice@korosUSA.com

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place at room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place at room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place at room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place at room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place at room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place at room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place at room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place at room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place at room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place at room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place at room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place at room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place at room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place at room temperature

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840199515769 [Direct Marking]
GS1	10840199515766 [Primary]

FDA Product Code

• FZX: Guide, Surgical, Instrument

Sterilization

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

[00840199515769]

Moist Heat or Steam Sterilization

[00840199515769]

Moist Heat or Steam Sterilization

[00840199515769]

Moist Heat or Steam Sterilization

[00840199515769]

Moist Heat or Steam Sterilization

[00840199515769]

Moist Heat or Steam Sterilization

[00840199515769]

Moist Heat or Steam Sterilization

[00840199515769]

Moist Heat or Steam Sterilization

[00840199515769]

Moist Heat or Steam Sterilization

[00840199515769]

Moist Heat or Steam Sterilization

[00840199515769]

Moist Heat or Steam Sterilization

[00840199515769]

Moist Heat or Steam Sterilization

[00840199515769]

Moist Heat or Steam Sterilization

[00840199515769]

Moist Heat or Steam Sterilization

[00840199515769]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-01-08
• Device Publish Date: 2024-12-31

On-Brand Devices [Distraction Screw Pre-Drill]

• 00840199515769: Anterior Lumbar Distraction Screw Pre-Drill 4.5mm
• 00840199515752: Anterior Lumbar Distraction Screw Pre-Drill 3.5mm
• 00840199515660: Distraction Screw Pre-Drill
• 00840199515639: Distraction Screw Pre-Drill
• 00840199515493: Tilting Arm Distraction Screw Pre-Drill