KYPHON Xpander™ II Inflatable Bone Tamp

GUDID 00643169093676

BONE TAMP KX203 20/3 XPANDER II IBT

MEDTRONIC SOFAMOR DANEK, INC.

Inflatable bone tamp

• Primary Device ID: 00643169093676
• NIH Device Record Key: 206b654c-900d-4686-aab2-57f7438aa5f7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: KYPHON Xpander™ II Inflatable Bone Tamp
• Version Model Number: KX203
• 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: 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	00643169093676 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K101864

FDA Product Code

• HXG: TAMP

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-04-02

On-Brand Devices [KYPHON Xpander™ II Inflatable Bone Tamp]

• 00643169093676: BONE TAMP KX203 20/3 XPANDER II IBT
• 00643169093652: BONE TAMP KX153 15/3 XPANDER II IBT
• 00643169093645: BONE TAMP KX103-C 10/3 XPANDER II IBT EU
• 00643169093638: BONE TAMP KX103 10/3 XPANDER II IBT