RELIEVE

GUDID 00889095040678

RELIEVE 2.2mm Screw, Self-Tapping, 6mm

GLOBUS MEDICAL, INC.

Spinal fixation plate, non-bioabsorbable

• Primary Device ID: 00889095040678
• NIH Device Record Key: 03870809-32da-436e-b674-3b6be6b0355c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RELIEVE
• Version Model Number: 136.506
• Company DUNS: 139105691
• Company Name: GLOBUS MEDICAL, INC.
• 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: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(610)930-1800
• Email: info@globusmedical.com
• Phone: +1(610)930-1800
• Email: info@globusmedical.com
• Phone: +1(610)930-1800
• Email: info@globusmedical.com
• Phone: +1(610)930-1800
• Email: info@globusmedical.com
• Phone: +1(610)930-1800
• Email: info@globusmedical.com
• Phone: +1(610)930-1800
• Email: info@globusmedical.com
• Phone: +1(610)930-1800
• Email: info@globusmedical.com
• Phone: +1(610)930-1800
• Email: info@globusmedical.com
• Phone: +1(610)930-1800
• Email: info@globusmedical.com
• Phone: +1(610)930-1800
• Email: info@globusmedical.com
• Phone: +1(610)930-1800
• Email: info@globusmedical.com
• Phone: +1(610)930-1800
• Email: info@globusmedical.com
• Phone: +1(610)930-1800
• Email: info@globusmedical.com
• Phone: +1(610)930-1800
• Email: info@globusmedical.com

Device Dimensions

• Outer Diameter: 2.2 Millimeter
• Length: 6 Millimeter
• Outer Diameter: 2.2 Millimeter
• Length: 6 Millimeter
• Outer Diameter: 2.2 Millimeter
• Length: 6 Millimeter
• Outer Diameter: 2.2 Millimeter
• Length: 6 Millimeter
• Outer Diameter: 2.2 Millimeter
• Length: 6 Millimeter
• Outer Diameter: 2.2 Millimeter
• Length: 6 Millimeter
• Outer Diameter: 2.2 Millimeter
• Length: 6 Millimeter
• Outer Diameter: 2.2 Millimeter
• Length: 6 Millimeter
• Outer Diameter: 2.2 Millimeter
• Length: 6 Millimeter
• Outer Diameter: 2.2 Millimeter
• Length: 6 Millimeter
• Outer Diameter: 2.2 Millimeter
• Length: 6 Millimeter
• Outer Diameter: 2.2 Millimeter
• Length: 6 Millimeter
• Outer Diameter: 2.2 Millimeter
• Length: 6 Millimeter
• Outer Diameter: 2.2 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00889095040678 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K080664

FDA Product Code

• NQW: ORTHOSIS, SPINE, PLATE, LAMINOPLASTY, METAL

Sterilization

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

[00889095040678]

Moist Heat or Steam Sterilization

[00889095040678]

Moist Heat or Steam Sterilization

[00889095040678]

Moist Heat or Steam Sterilization

[00889095040678]

Moist Heat or Steam Sterilization

[00889095040678]

Moist Heat or Steam Sterilization

[00889095040678]

Moist Heat or Steam Sterilization

[00889095040678]

Moist Heat or Steam Sterilization

[00889095040678]

Moist Heat or Steam Sterilization

[00889095040678]

Moist Heat or Steam Sterilization

[00889095040678]

Moist Heat or Steam Sterilization

[00889095040678]

Moist Heat or Steam Sterilization

[00889095040678]

Moist Heat or Steam Sterilization

[00889095040678]

Moist Heat or Steam Sterilization

[00889095040678]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-10-01

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