LOW PROFILE CROSSLINK(R) System

GUDID 00673978157047

LPX CONN DOM-TI-O/C-6.35/6.35

MEDTRONIC SOFAMOR DANEK, INC.

Bone-screw internal spinal fixation system, non-sterile

• Primary Device ID: 00673978157047
• NIH Device Record Key: 98551ebe-2cb7-487a-b674-abf7a6543488
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LOW PROFILE CROSSLINK(R) System
• Version Model Number: X1298-026
• 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: 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
• 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 Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00673978157047 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K955365

FDA Product Code

• KWP: APPLIANCE, FIXATION, SPINAL INTERLAMINAL

Sterilization

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

[00673978157047]

Moist Heat or Steam Sterilization

[00673978157047]

Moist Heat or Steam Sterilization

[00673978157047]

Moist Heat or Steam Sterilization

[00673978157047]

Moist Heat or Steam Sterilization

[00673978157047]

Moist Heat or Steam Sterilization

[00673978157047]

Moist Heat or Steam Sterilization

[00673978157047]

Moist Heat or Steam Sterilization

[00673978157047]

Moist Heat or Steam Sterilization

[00673978157047]

Moist Heat or Steam Sterilization

[00673978157047]

Moist Heat or Steam Sterilization

[00673978157047]

Moist Heat or Steam Sterilization

[00673978157047]

Moist Heat or Steam Sterilization

[00673978157047]

Moist Heat or Steam Sterilization

[00673978157047]

Moist Heat or Steam Sterilization

[00673978157047]

Moist Heat or Steam Sterilization

[00673978157047]

Moist Heat or Steam Sterilization

[00673978157047]

Moist Heat or Steam Sterilization

[00673978157047]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-08-19

On-Brand Devices [LOW PROFILE CROSSLINK(R) System]

• 00673978157047: LPX CONN DOM-TI-O/C-6.35/6.35
• 00673978156330: LPX MSLNK 5.5/6.35 2.15-2.9 SS
• 00673978156323: LPX MSLNK 5.5/6.35 1.75-2.1 SS
• 00673978156316: LPX MSLNK 5.5/6.35 1.55-1.7 SS