PREFERENCE Pedicle Screw System

GUDID 00841732145122

Lateral Connector Caddy

CTL Medical Corporation

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• Primary Device ID: 00841732145122
• NIH Device Record Key: ff2924e8-571d-4b1e-885c-76d3b4829ede
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PREFERENCE Pedicle Screw System
• Version Model Number: 055.8303
• Company DUNS: 080138504
• Company Name: CTL Medical Corporation
• 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: true
• 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 (214) 545-5820
• Email: schedule@ctlamedica.com
• Phone: 1 (214) 545-5820
• Email: schedule@ctlamedica.com
• Phone: 1 (214) 545-5820
• Email: schedule@ctlamedica.com
• Phone: 1 (214) 545-5820
• Email: schedule@ctlamedica.com
• Phone: 1 (214) 545-5820
• Email: schedule@ctlamedica.com
• Phone: 1 (214) 545-5820
• Email: schedule@ctlamedica.com
• Phone: 1 (214) 545-5820
• Email: schedule@ctlamedica.com
• Phone: 1 (214) 545-5820
• Email: schedule@ctlamedica.com
• Phone: 1 (214) 545-5820
• Email: schedule@ctlamedica.com
• Phone: 1 (214) 545-5820
• Email: schedule@ctlamedica.com
• Phone: 1 (214) 545-5820
• Email: schedule@ctlamedica.com
• Phone: 1 (214) 545-5820
• Email: schedule@ctlamedica.com
• Phone: 1 (214) 545-5820
• Email: schedule@ctlamedica.com
• Phone: 1 (214) 545-5820
• Email: schedule@ctlamedica.com
• Phone: 1 (214) 545-5820
• Email: schedule@ctlamedica.com
• Phone: 1 (214) 545-5820
• Email: schedule@ctlamedica.com
• Phone: 1 (214) 545-5820
• Email: schedule@ctlamedica.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841732145122 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K081296

FDA Product Code

• KWP: Appliance, Fixation, Spinal Interlaminal

Sterilization

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

[00841732145122]

Moist Heat or Steam Sterilization

[00841732145122]

Moist Heat or Steam Sterilization

[00841732145122]

Moist Heat or Steam Sterilization

[00841732145122]

Moist Heat or Steam Sterilization

[00841732145122]

Moist Heat or Steam Sterilization

[00841732145122]

Moist Heat or Steam Sterilization

[00841732145122]

Moist Heat or Steam Sterilization

[00841732145122]

Moist Heat or Steam Sterilization

[00841732145122]

Moist Heat or Steam Sterilization

[00841732145122]

Moist Heat or Steam Sterilization

[00841732145122]

Moist Heat or Steam Sterilization

[00841732145122]

Moist Heat or Steam Sterilization

[00841732145122]

Moist Heat or Steam Sterilization

[00841732145122]

Moist Heat or Steam Sterilization

[00841732145122]

Moist Heat or Steam Sterilization

[00841732145122]

Moist Heat or Steam Sterilization

[00841732145122]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-07-01
• Device Publish Date: 2024-06-21

On-Brand Devices [PREFERENCE Pedicle Screw System]

• 00841732145139: Connector Caddy- Fixed
• 00841732145122: Lateral Connector Caddy
• 00841732145115: Domino Connector Caddy