AEKA60R17

GUDID 00841379138877

ROD EXTENSION CONNECTOR, SIDE LOADING

HYHTE HOLDINGS, INC.

Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile

• Primary Device ID: 00841379138877
• NIH Device Record Key: 336be5bd-f301-4484-a27f-7b012d0d18d7
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: AEKA60R17
• Catalog Number: AEKA60R17
• 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

• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 6 Millimeter
• Width: 6 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 6 Millimeter
• Width: 6 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 6 Millimeter
• Width: 6 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 6 Millimeter
• Width: 6 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 6 Millimeter
• Width: 6 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 6 Millimeter
• Width: 6 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 6 Millimeter
• Width: 6 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 6 Millimeter
• Width: 6 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 6 Millimeter
• Width: 6 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 6 Millimeter
• Width: 6 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 6 Millimeter
• Width: 6 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 6 Millimeter
• Width: 6 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 6 Millimeter
• Width: 6 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 6 Millimeter
• Width: 6 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 6 Millimeter
• Width: 6 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 6 Millimeter
• Width: 6 Millimeter
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841379138877 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K153446

FDA Product Code

• OSH: Pedicle Screw Spinal System, Adolescent Idiopathic Scoliosis

Sterilization

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

[00841379138877]

Moist Heat or Steam Sterilization

[00841379138877]

Moist Heat or Steam Sterilization

[00841379138877]

Moist Heat or Steam Sterilization

[00841379138877]

Moist Heat or Steam Sterilization

[00841379138877]

Moist Heat or Steam Sterilization

[00841379138877]

Moist Heat or Steam Sterilization

[00841379138877]

Moist Heat or Steam Sterilization

[00841379138877]

Moist Heat or Steam Sterilization

[00841379138877]

Moist Heat or Steam Sterilization

[00841379138877]

Moist Heat or Steam Sterilization

[00841379138877]

Moist Heat or Steam Sterilization

[00841379138877]

Moist Heat or Steam Sterilization

[00841379138877]

Moist Heat or Steam Sterilization

[00841379138877]

Moist Heat or Steam Sterilization

[00841379138877]

Moist Heat or Steam Sterilization

[00841379138877]

Moist Heat or Steam Sterilization

[00841379138877]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-07-23
• Device Publish Date: 2018-06-22

Devices Manufactured by HYHTE HOLDINGS, INC.

• 00840085254413 - NA: 2024-05-07 POLYAXIAL, TULIP
• 00840085254420 - NA: 2024-05-07 POLYAXIAL, HIGH TOP, TULIP
• 00840085254437 - NA: 2024-05-07 POLYAXIAL, EXTENDED TAB, TULIP
• 00840085254444 - NA: 2024-05-07 FAVORED ANGLE M/L, TULIP
• 00840085254451 - NA: 2024-05-07 FAVORED ANGLE M/L, HIGH TOP, TULIP
• 00840085254468 - NA: 2024-05-07 FAVORED ANGLE M/L, EXTENED TAB, TULIP
• 00840085254475 - NA: 2024-05-07 FAVORED ANGLE C/C, TULIP
• 00840085254482 - NA: 2024-05-07 FAVORED ANGLE C/C, HIGH TOP, TULIP