CATALYST® Reusable Instruments

GUDID 00885074058153

INSTRUMENT 3289810 OBL PREC SPREADR 10MM

MEDTRONIC SOFAMOR DANEK, INC.

Orthopaedic prosthesis implantation instrument, reusable

• Primary Device ID: 00885074058153
• NIH Device Record Key: 59966af0-c808-4e0c-9735-53a332d176f6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CATALYST® Reusable Instruments
• Version Model Number: 3289810
• 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: false
• 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

Device Dimensions

• 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 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	00885074058153 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K090353

FDA Product Code

• MAX: Intervertebral fusion device with bone graft, lumbar

Sterilization

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

[00885074058153]

Moist Heat or Steam Sterilization

[00885074058153]

Moist Heat or Steam Sterilization

[00885074058153]

Moist Heat or Steam Sterilization

[00885074058153]

Moist Heat or Steam Sterilization

[00885074058153]

Moist Heat or Steam Sterilization

[00885074058153]

Moist Heat or Steam Sterilization

[00885074058153]

Moist Heat or Steam Sterilization

[00885074058153]

Moist Heat or Steam Sterilization

[00885074058153]

Moist Heat or Steam Sterilization

[00885074058153]

Moist Heat or Steam Sterilization

[00885074058153]

Moist Heat or Steam Sterilization

[00885074058153]

Moist Heat or Steam Sterilization

[00885074058153]

Moist Heat or Steam Sterilization

[00885074058153]

Moist Heat or Steam Sterilization

[00885074058153]

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: 2015-08-07

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• 00763000889227 - ATLANTIS® Anterior Cervical Plate System: 2025-06-06 SCREW 3125313 4.5 X 13 SELF TAP VAR
• 00763000889319 - ATLANTIS® Anterior Cervical Plate System: 2025-06-06 SCREW 3120214 4.0 X 14 SELF TAP FIX
• 00763000889425 - ATLANTIS® Anterior Cervical Plate System: 2025-06-06 SCREW 3120514 4.0 X 14 SELF DRILL VAR