UNIT ROD

GUDID 00673978135649

S-ROD 4.76X51CM R SS

MEDTRONIC SOFAMOR DANEK, INC.

Bone-screw internal spinal fixation system, non-sterile

• Primary Device ID: 00673978135649
• NIH Device Record Key: f57f0452-17c3-4d0d-8555-3c3dcc9cb707
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: UNIT ROD
• Version Model Number: X0397-027
• Company DUNS: 830350380
• Company Name: MEDTRONIC SOFAMOR DANEK, 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: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
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• Device Size Text, specify: 0
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• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
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• Device Size Text, specify: 0
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• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00673978135649 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K110676

FDA Product Code

• KWP: APPLIANCE, FIXATION, SPINAL INTERLAMINAL

Sterilization

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

[00673978135649]

Moist Heat or Steam Sterilization

[00673978135649]

Moist Heat or Steam Sterilization

[00673978135649]

Moist Heat or Steam Sterilization

[00673978135649]

Moist Heat or Steam Sterilization

[00673978135649]

Moist Heat or Steam Sterilization

[00673978135649]

Moist Heat or Steam Sterilization

[00673978135649]

Moist Heat or Steam Sterilization

[00673978135649]

Moist Heat or Steam Sterilization

[00673978135649]

Moist Heat or Steam Sterilization

[00673978135649]

Moist Heat or Steam Sterilization

[00673978135649]

Moist Heat or Steam Sterilization

[00673978135649]

Moist Heat or Steam Sterilization

[00673978135649]

Moist Heat or Steam Sterilization

[00673978135649]

Moist Heat or Steam Sterilization

[00673978135649]

Moist Heat or Steam Sterilization

[00673978135649]

Moist Heat or Steam Sterilization

[00673978135649]

Moist Heat or Steam Sterilization

[00673978135649]

Moist Heat or Steam Sterilization

[00673978135649]

Moist Heat or Steam Sterilization

[00673978135649]

Moist Heat or Steam Sterilization

[00673978135649]

Moist Heat or Steam Sterilization

[00673978135649]

Moist Heat or Steam Sterilization

[00673978135649]

Moist Heat or Steam Sterilization

[00673978135649]

Moist Heat or Steam Sterilization

[00673978135649]

Moist Heat or Steam Sterilization

[00673978135649]

Moist Heat or Steam Sterilization

[00673978135649]

Moist Heat or Steam Sterilization

[00673978135649]

Moist Heat or Steam Sterilization

[00673978135649]

Moist Heat or Steam Sterilization

[00673978135649]

Moist Heat or Steam Sterilization

[00673978135649]

Moist Heat or Steam Sterilization

[00673978135649]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-08-24

On-Brand Devices [UNIT ROD]

• 00673978159690: UNIT ROD 6.35X27CM SS
• 00673978135649: S-ROD 4.76X51CM R SS
• 00673978135632: S-ROD 4.76X51CM L SS