ConneX Rod Connector 680-5501

GUDID M7406805501

Rod Connector, Axial

SPINEOLOGY INC.

Bone-screw internal spinal fixation system rod

• Primary Device ID: M7406805501
• NIH Device Record Key: 040db66e-5cdc-454b-a841-99f053de35b3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ConneX Rod Connector
• Version Model Number: 10-10-82-11
• Catalog Number: 680-5501
• Company DUNS: 033014361
• Company Name: SPINEOLOGY INC.
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• 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: true
• 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: +1(651)259-8500
• Email: info@spineology.com
• Phone: +1(651)259-8500
• Email: info@spineology.com
• Phone: +1(651)259-8500
• Email: info@spineology.com
• Phone: +1(651)259-8500
• Email: info@spineology.com
• Phone: +1(651)259-8500
• Email: info@spineology.com
• Phone: +1(651)259-8500
• Email: info@spineology.com
• Phone: +1(651)259-8500
• Email: info@spineology.com
• Phone: +1(651)259-8500
• Email: info@spineology.com
• Phone: +1(651)259-8500
• Email: info@spineology.com
• Phone: +1(651)259-8500
• Email: info@spineology.com
• Phone: +1(651)259-8500
• Email: info@spineology.com
• Phone: +1(651)259-8500
• Email: info@spineology.com
• Phone: +1(651)259-8500
• Email: info@spineology.com
• Phone: +1(651)259-8500
• Email: info@spineology.com
• Phone: +1(651)259-8500
• Email: info@spineology.com
• Phone: +1(651)259-8500
• Email: info@spineology.com
• Phone: +1(651)259-8500
• Email: info@spineology.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	M7406805501 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K170251

FDA Product Code

• MNI: ORTHOSIS, SPINAL PEDICLE FIXATION

Sterilization

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

[M7406805501]

Ethylene Oxide

[M7406805501]

Ethylene Oxide

[M7406805501]

Ethylene Oxide

[M7406805501]

Ethylene Oxide

[M7406805501]

Ethylene Oxide

[M7406805501]

Ethylene Oxide

[M7406805501]

Ethylene Oxide

[M7406805501]

Ethylene Oxide

[M7406805501]

Ethylene Oxide

[M7406805501]

Ethylene Oxide

[M7406805501]

Ethylene Oxide

[M7406805501]

Ethylene Oxide

[M7406805501]

Ethylene Oxide

[M7406805501]

Ethylene Oxide

[M7406805501]

Ethylene Oxide

[M7406805501]

Ethylene Oxide

[M7406805501]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2024-07-22
• Device Publish Date: 2017-04-25

On-Brand Devices [ConneX Rod Connector]

• M7406805502: Rod Connector, Parallel
• M7406805501: Rod Connector, Axial
• M7406800016: Rod Connector, Offset
• M7406800013: Rod Connector, Offset