RELIEVE

GUDID 00889095215366

RELIEVE Radiolucent Plate, Open Door, Widemouth, 13mm

GLOBUS MEDICAL, INC.

Spinal fixation plate, non-bioabsorbable

• Primary Device ID: 00889095215366
• NIH Device Record Key: 1599824a-6447-4af5-b0c3-f4982f634471
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RELIEVE
• Version Model Number: 336.313
• 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

Device Dimensions

• Height: 13 Millimeter
• Height: 13 Millimeter
• Height: 13 Millimeter
• Height: 13 Millimeter
• Height: 13 Millimeter
• Height: 13 Millimeter
• Height: 13 Millimeter
• Height: 13 Millimeter
• Height: 13 Millimeter
• Height: 13 Millimeter
• Height: 13 Millimeter
• Height: 13 Millimeter
• Height: 13 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00889095215366 [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

[00889095215366]

Moist Heat or Steam Sterilization

[00889095215366]

Moist Heat or Steam Sterilization

[00889095215366]

Moist Heat or Steam Sterilization

[00889095215366]

Moist Heat or Steam Sterilization

[00889095215366]

Moist Heat or Steam Sterilization

[00889095215366]

Moist Heat or Steam Sterilization

[00889095215366]

Moist Heat or Steam Sterilization

[00889095215366]

Moist Heat or Steam Sterilization

[00889095215366]

Moist Heat or Steam Sterilization

[00889095215366]

Moist Heat or Steam Sterilization

[00889095215366]

Moist Heat or Steam Sterilization

[00889095215366]

Moist Heat or Steam Sterilization

[00889095215366]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2023-09-18
• Device Publish Date: 2015-11-06

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