Express™ Osteo Introducer® System; CDS and BFD

GUDID 00763000557102

KIT KEX202EB-CDS-A 20/2 FF W CDS

MEDTRONIC SOFAMOR DANEK, INC.

Balloon kyphoplasty kit

• Primary Device ID: 00763000557102
• NIH Device Record Key: 6077a246-1a01-4875-910e-3c298a4e38fc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Express™ Osteo Introducer® System; CDS and BFD
• Version Model Number: KEX202EB-CDS-A
• Company DUNS: 830350380
• Company Name: MEDTRONIC SOFAMOR DANEK, INC.
• Device Count: 1
• DM Exempt: true
• 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

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool dry place
• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool dry place
• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool dry place
• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool dry place
• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool dry place
• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool dry place
• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool dry place
• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool dry place
• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool dry place

Device Identifiers

Device Issuing Agency	Device ID
GS1	00763000557102 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K123771

FDA Product Code

• HRX: Arthroscope

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-08-17
• Device Publish Date: 2021-08-09

On-Brand Devices [Express™ Osteo Introducer® System; CDS and BFD]

• 00763000557102: KIT KEX202EB-CDS-A 20/2 FF W CDS
• 00763000557096: KIT KEX152EB-CDS-A 15/2 FF W CDS
• 00763000557089: KIT KEX102EB-CDS-A 10/2 FF W CDS