Fusion™ ENT Image Guidance System

GUDID 00613994594235

System 9733560XOMR Fusion Refurb

MEDTRONIC NAVIGATION, INC.

ENT stereotactic surgery system

• Primary Device ID: 00613994594235
• NIH Device Record Key: 8a61980f-6fc4-4ff8-9c10-fc5b4ecaf670
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Fusion™ ENT Image Guidance System
• Version Model Number: 9733560XOMR
• Company DUNS: 835233107
• Company Name: MEDTRONIC NAVIGATION, 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: false
• Serial Number: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00613994594235 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K001284

FDA Product Code

• HAW: Neurological stereotaxic Instrument

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-03-05
• Device Publish Date: 2016-05-27

On-Brand Devices [Fusion™ ENT Image Guidance System]

• 00613994594235: System 9733560XOMR Fusion Refurb
• 00613994380005: CART 9733560XOM FUSION EM SYSTEM
• 00643169518452: SYSTEM 9733560XOM FUSION EM
• 00643169504394: SYSTEM 9733560 FUSION EM
• 00763000235079: SYSTEM 9733560 FUSION EM