KYPHON® Directional Bone Filler Device

GUDID 00643169097230

BONE FILLER DEVICE F04C DIRECT SIZE 3

MEDTRONIC SOFAMOR DANEK, INC.

Orthopaedic cement dispenser

• Primary Device ID: 00643169097230
• NIH Device Record Key: 0ce55670-916e-41f5-8520-cd665ccc12d4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: KYPHON® Directional Bone Filler Device
• Version Model Number: F04C
• Company DUNS: 830350380
• Company Name: MEDTRONIC SOFAMOR DANEK, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00643169097230 [Primary]

FDA Product Code

• KIH: DISPENSER, CEMENT

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-11-26

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