KJC21000C

GUDID 00840085249020

OBLIQUE ALIF PLATE, LI-RS HALF

HYHTE HOLDINGS, INC.

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• Primary Device ID: 00840085249020
• NIH Device Record Key: 18814f61-5cb1-4a33-826a-eb1eef6e4d09
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: KJC21000C
• Catalog Number: KJC21000C
• Company DUNS: 073029645
• Company Name: HYHTE HOLDINGS, 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 7608148047
• Email: PARKER@ASTURAMEDICAL.COM
• Phone: 7608148047
• Email: PARKER@ASTURAMEDICAL.COM
• Phone: 7608148047
• Email: PARKER@ASTURAMEDICAL.COM
• Phone: 7608148047
• Email: PARKER@ASTURAMEDICAL.COM
• Phone: 7608148047
• Email: PARKER@ASTURAMEDICAL.COM
• Phone: 7608148047
• Email: PARKER@ASTURAMEDICAL.COM
• Phone: 7608148047
• Email: PARKER@ASTURAMEDICAL.COM
• Phone: 7608148047
• Email: PARKER@ASTURAMEDICAL.COM
• Phone: 7608148047
• Email: PARKER@ASTURAMEDICAL.COM
• Phone: 7608148047
• Email: PARKER@ASTURAMEDICAL.COM
• Phone: 7608148047
• Email: PARKER@ASTURAMEDICAL.COM
• Phone: 7608148047
• Email: PARKER@ASTURAMEDICAL.COM

Device Dimensions

• Height: 21 Millimeter
• Angle: 20 degree
• Height: 21 Millimeter
• Angle: 20 degree
• Height: 21 Millimeter
• Angle: 20 degree
• Height: 21 Millimeter
• Angle: 20 degree
• Height: 21 Millimeter
• Angle: 20 degree
• Height: 21 Millimeter
• Angle: 20 degree
• Height: 21 Millimeter
• Angle: 20 degree
• Height: 21 Millimeter
• Angle: 20 degree
• Height: 21 Millimeter
• Angle: 20 degree
• Height: 21 Millimeter
• Angle: 20 degree
• Height: 21 Millimeter
• Angle: 20 degree
• Height: 21 Millimeter
• Angle: 20 degree

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840085249020 [Primary]

FDA Product Code

• OVD: Intervertebral Fusion Device With Integrated Fixation, Lumbar

Sterilization

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

[00840085249020]

Moist Heat or Steam Sterilization

[00840085249020]

Moist Heat or Steam Sterilization

[00840085249020]

Moist Heat or Steam Sterilization

[00840085249020]

Moist Heat or Steam Sterilization

[00840085249020]

Moist Heat or Steam Sterilization

[00840085249020]

Moist Heat or Steam Sterilization

[00840085249020]

Moist Heat or Steam Sterilization

[00840085249020]

Moist Heat or Steam Sterilization

[00840085249020]

Moist Heat or Steam Sterilization

[00840085249020]

Moist Heat or Steam Sterilization

[00840085249020]

Moist Heat or Steam Sterilization

[00840085249020]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-05-16
• Device Publish Date: 2022-05-06

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• 00840085257483 - NA: 2024-04-18 DUAL LEAD SCREW
• 00840085257490 - NA: 2024-04-18 DUAL LEAD SCREW
• 00840085257506 - NA: 2024-04-18 DUAL LEAD SCREW
• 00840085257513 - NA: 2024-04-18 DUAL LEAD SCREW
• 00840085257520 - NA: 2024-04-18 DUAL LEAD SCREW
• 00840085257537 - NA: 2024-04-18 DUAL LEAD SCREW