Fusion™ ENT Image Guidance System

GUDID 00763000235079

SYSTEM 9733560 FUSION EM

MEDTRONIC NAVIGATION, INC.

ENT stereotactic surgery system

• Primary Device ID: 00763000235079
• NIH Device Record Key: d3d6fcc8-5f58-4e77-8523-8d96497f2518
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Fusion™ ENT Image Guidance System
• Version Model Number: 9733560
• 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: 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00763000235079 [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: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-02-25
• Device Publish Date: 2019-01-24

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