AJFA95100

GUDID 00841379171683

LRG DIA POLYAXIAL SCREW, CANN, SELF CUTTING,

HYHTE HOLDINGS, INC.

Spinal bone screw, non-bioabsorbable

• Primary Device ID: 00841379171683
• NIH Device Record Key: 9b21cb23-6b8f-4979-a2f1-94d3975512f3
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: AJFA95100
• Catalog Number: AJFA95100
• 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
• 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

• Outer Diameter: 9.5 Millimeter
• Length: 100 Millimeter
• Outer Diameter: 9.5 Millimeter
• Length: 100 Millimeter
• Outer Diameter: 9.5 Millimeter
• Length: 100 Millimeter
• Outer Diameter: 9.5 Millimeter
• Length: 100 Millimeter
• Outer Diameter: 9.5 Millimeter
• Length: 100 Millimeter
• Outer Diameter: 9.5 Millimeter
• Length: 100 Millimeter
• Outer Diameter: 9.5 Millimeter
• Length: 100 Millimeter
• Outer Diameter: 9.5 Millimeter
• Length: 100 Millimeter
• Outer Diameter: 9.5 Millimeter
• Length: 100 Millimeter
• Outer Diameter: 9.5 Millimeter
• Length: 100 Millimeter
• Outer Diameter: 9.5 Millimeter
• Length: 100 Millimeter
• Outer Diameter: 9.5 Millimeter
• Length: 100 Millimeter
• Outer Diameter: 9.5 Millimeter
• Length: 100 Millimeter
• Outer Diameter: 9.5 Millimeter
• Length: 100 Millimeter
• Outer Diameter: 9.5 Millimeter
• Length: 100 Millimeter
• Outer Diameter: 9.5 Millimeter
• Length: 100 Millimeter
• Outer Diameter: 9.5 Millimeter
• Length: 100 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841379171683 [Primary]

FDA Product Code

• NKB: Thoracolumbosacral Pedicle Screw System

Sterilization

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

[00841379171683]

Moist Heat or Steam Sterilization

[00841379171683]

Moist Heat or Steam Sterilization

[00841379171683]

Moist Heat or Steam Sterilization

[00841379171683]

Moist Heat or Steam Sterilization

[00841379171683]

Moist Heat or Steam Sterilization

[00841379171683]

Moist Heat or Steam Sterilization

[00841379171683]

Moist Heat or Steam Sterilization

[00841379171683]

Moist Heat or Steam Sterilization

[00841379171683]

Moist Heat or Steam Sterilization

[00841379171683]

Moist Heat or Steam Sterilization

[00841379171683]

Moist Heat or Steam Sterilization

[00841379171683]

Moist Heat or Steam Sterilization

[00841379171683]

Moist Heat or Steam Sterilization

[00841379171683]

Moist Heat or Steam Sterilization

[00841379171683]

Moist Heat or Steam Sterilization

[00841379171683]

Moist Heat or Steam Sterilization

[00841379171683]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2024-11-06
• Device Publish Date: 2021-05-28

Devices Manufactured by HYHTE HOLDINGS, INC.

• 00840085272509 - NA: 2024-11-06 ENDPLATE, 20MM, VARIABLE LORDISIS, LATERAL, FULL, R.
• 00840085273322 - NA: 2024-11-06 ENDPLATE, 16MM, VARIABLE LORDOSIS, LATERAL, FULL, L.
• 00840085273339 - NA: 2024-11-06 ENDPLATE, 16MM, VARIABLE LORDOSIS, LATERAL, FULL, L.
• 00840085273346 - NA: 2024-11-06 ENDPLATE, 16MM, VARIABLE LORDOSIS, LATERAL, FULL, L.
• 00840085273353 - NA: 2024-11-06 ENDPLATE, 16MM, VARIABLE LORDOSIS, LATERAL, FULL, L.
• 00840085273360 - NA: 2024-11-06 ENDPLATE, 16MM, VARIABLE LORDOSIS, LATERAL, FULL, L.
• 00840085273377 - NA: 2024-11-06 ENDPLATE, 16MM, VARIABLE LORDOSIS, LATERAL, FULL, L.
• 00840085273384 - NA: 2024-11-06 ENDPLATE, 16MM, VARIABLE LORDOSIS, LATERAL, FULL, L.