ConneX Cross Connector 680-2531

GUDID M7406802531

Cross Connector, Adjustable

SPINEOLOGY INC.

Bone-screw internal spinal fixation system rod

• Primary Device ID: M7406802531
• NIH Device Record Key: 02869c81-ee6f-454f-95e5-e01a12747696
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ConneX Cross Connector
• Version Model Number: 10-10-82-2
• Catalog Number: 680-2531
• 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 Dimensions

• Device Size Text, specify: 0
• Length: 25 Millimeter
• Device Size Text, specify: 0
• Length: 25 Millimeter
• Device Size Text, specify: 0
• Length: 25 Millimeter
• Device Size Text, specify: 0
• Length: 25 Millimeter
• Device Size Text, specify: 0
• Length: 25 Millimeter
• Device Size Text, specify: 0
• Length: 25 Millimeter
• Device Size Text, specify: 0
• Length: 25 Millimeter
• Device Size Text, specify: 0
• Length: 25 Millimeter
• Device Size Text, specify: 0
• Length: 25 Millimeter
• Device Size Text, specify: 0
• Length: 25 Millimeter
• Device Size Text, specify: 0
• Length: 25 Millimeter
• Device Size Text, specify: 0
• Length: 25 Millimeter
• Device Size Text, specify: 0
• Length: 25 Millimeter
• Device Size Text, specify: 0
• Length: 25 Millimeter
• Device Size Text, specify: 0
• Length: 25 Millimeter
• Device Size Text, specify: 0
• Length: 25 Millimeter
• Device Size Text, specify: 0
• Length: 25 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	M7406802531 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K170251

FDA Product Code

• MNH: Orthosis, spondylolisthesis spinal fixation

Sterilization

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

[M7406802531]

Ethylene Oxide

[M7406802531]

Ethylene Oxide

[M7406802531]

Ethylene Oxide

[M7406802531]

Ethylene Oxide

[M7406802531]

Ethylene Oxide

[M7406802531]

Ethylene Oxide

[M7406802531]

Ethylene Oxide

[M7406802531]

Ethylene Oxide

[M7406802531]

Ethylene Oxide

[M7406802531]

Ethylene Oxide

[M7406802531]

Ethylene Oxide

[M7406802531]

Ethylene Oxide

[M7406802531]

Ethylene Oxide

[M7406802531]

Ethylene Oxide

[M7406802531]

Ethylene Oxide

[M7406802531]

Ethylene Oxide

[M7406802531]

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

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