CoreLink LATERAL PLATE - 2 SCREW

GUDID M72590021520

LATERAL PLATE - 2 SCREW, 15MM X 20MM

CORELINK LLC

Spinal fixation plate, non-bioabsorbable

• Primary Device ID: M72590021520
• NIH Device Record Key: f242a14d-58ce-4d0d-ad78-1709411fc7e9
• Commercial Distribution Discontinuation: 2025-01-03
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: CoreLink LATERAL PLATE - 2 SCREW
• Version Model Number: 900215-20
• Company DUNS: 064191453
• Company Name: CORELINK 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: true
• 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

Customer Support Contacts

• Phone: 6019191119
• Email: info@zavation.com
• Phone: 6019191119
• Email: info@zavation.com
• Phone: 6019191119
• Email: info@zavation.com
• Phone: 6019191119
• Email: info@zavation.com
• Phone: 6019191119
• Email: info@zavation.com
• Phone: 6019191119
• Email: info@zavation.com
• Phone: 6019191119
• Email: info@zavation.com
• Phone: 6019191119
• Email: info@zavation.com
• Phone: 6019191119
• Email: info@zavation.com
• Phone: 6019191119
• Email: info@zavation.com
• Phone: 6019191119
• Email: info@zavation.com
• Phone: 6019191119
• Email: info@zavation.com
• Phone: 6019191119
• Email: info@zavation.com
• Phone: 6019191119
• Email: info@zavation.com
• Phone: 6019191119
• Email: info@zavation.com
• Phone: 6019191119
• Email: info@zavation.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	M72590021520 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K190016

FDA Product Code

• KWQ: Appliance, Fixation, Spinal Intervertebral Body

Sterilization

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

[M72590021520]

Moist Heat or Steam Sterilization

[M72590021520]

Moist Heat or Steam Sterilization

[M72590021520]

Moist Heat or Steam Sterilization

[M72590021520]

Moist Heat or Steam Sterilization

[M72590021520]

Moist Heat or Steam Sterilization

[M72590021520]

Moist Heat or Steam Sterilization

[M72590021520]

Moist Heat or Steam Sterilization

[M72590021520]

Moist Heat or Steam Sterilization

[M72590021520]

Moist Heat or Steam Sterilization

[M72590021520]

Moist Heat or Steam Sterilization

[M72590021520]

Moist Heat or Steam Sterilization

[M72590021520]

Moist Heat or Steam Sterilization

[M72590021520]

Moist Heat or Steam Sterilization

[M72590021520]

Moist Heat or Steam Sterilization

[M72590021520]

Moist Heat or Steam Sterilization

[M72590021520]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-01-13
• Device Publish Date: 2025-01-03

On-Brand Devices [CoreLink LATERAL PLATE - 2 SCREW]

• M72590021520: LATERAL PLATE - 2 SCREW, 15MM X 20MM
• M72590021518: LATERAL PLATE - 2 SCREW, 15MM X 18MM
• M72590021516: LATERAL PLATE - 2 SCREW, 15MM X 16MM