LIBERTY® Posterior Spinal System

GUDID 00721902515149

CONNECTOR X0602030 L S C S 6.35 4.5 30MM

MEDTRONIC SOFAMOR DANEK, INC.

Bone-screw internal spinal fixation system, non-sterile

• Primary Device ID: 00721902515149
• NIH Device Record Key: cd23630d-ab6e-48d9-b3e6-be4310265e53
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LIBERTY® Posterior Spinal System
• Version Model Number: X0602030
• 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
• 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

• Outer Diameter: 4.5 Millimeter
• Outer Diameter: 4.5 Millimeter
• Outer Diameter: 4.5 Millimeter
• Outer Diameter: 4.5 Millimeter
• Length: 30 Millimeter
• Outer Diameter: 4.5 Millimeter
• Length: 30 Millimeter
• Outer Diameter: 4.5 Millimeter
• Length: 30 Millimeter
• Outer Diameter: 4.5 Millimeter
• Length: 30 Millimeter
• Outer Diameter: 4.5 Millimeter
• Length: 30 Millimeter
• Outer Diameter: 4.5 Millimeter
• Length: 30 Millimeter
• Outer Diameter: 4.5 Millimeter
• Length: 30 Millimeter
• Outer Diameter: 4.5 Millimeter
• Length: 30 Millimeter
• Outer Diameter: 4.5 Millimeter
• Length: 30 Millimeter
• Outer Diameter: 4.5 Millimeter
• Length: 30 Millimeter
• Outer Diameter: 4.5 Millimeter
• Length: 30 Millimeter
• Outer Diameter: 4.5 Millimeter
• Length: 30 Millimeter
• Outer Diameter: 4.5 Millimeter
• Length: 30 Millimeter
• Outer Diameter: 4.5 Millimeter
• Length: 30 Millimeter
• Outer Diameter: 4.5 Millimeter
• Length: 30 Millimeter
• Outer Diameter: 4.5 Millimeter
• Length: 30 Millimeter
• Outer Diameter: 4.5 Millimeter
• Length: 30 Millimeter
• Outer Diameter: 4.5 Millimeter
• Length: 30 Millimeter
• Outer Diameter: 4.5 Millimeter
• Length: 30 Millimeter
• Outer Diameter: 4.5 Millimeter
• Length: 30 Millimeter
• Outer Diameter: 4.5 Millimeter
• Length: 30 Millimeter
• Outer Diameter: 4.5 Millimeter
• Length: 30 Millimeter
• Outer Diameter: 4.5 Millimeter
• Length: 30 Millimeter
• Outer Diameter: 4.5 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00721902515149 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K951164

FDA Product Code

• MNH: Orthosis, spondylolisthesis spinal fixation

Sterilization

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

[00721902515149]

Moist Heat or Steam Sterilization

[00721902515149]

Moist Heat or Steam Sterilization

[00721902515149]

Moist Heat or Steam Sterilization

[00721902515149]

Moist Heat or Steam Sterilization

[00721902515149]

Moist Heat or Steam Sterilization

[00721902515149]

Moist Heat or Steam Sterilization

[00721902515149]

Moist Heat or Steam Sterilization

[00721902515149]

Moist Heat or Steam Sterilization

[00721902515149]

Moist Heat or Steam Sterilization

[00721902515149]

Moist Heat or Steam Sterilization

[00721902515149]

Moist Heat or Steam Sterilization

[00721902515149]

Moist Heat or Steam Sterilization

[00721902515149]

Moist Heat or Steam Sterilization

[00721902515149]

Moist Heat or Steam Sterilization

[00721902515149]

Moist Heat or Steam Sterilization

[00721902515149]

Moist Heat or Steam Sterilization

[00721902515149]

Moist Heat or Steam Sterilization

[00721902515149]

Moist Heat or Steam Sterilization

[00721902515149]

Moist Heat or Steam Sterilization

[00721902515149]

Moist Heat or Steam Sterilization

[00721902515149]

Moist Heat or Steam Sterilization

[00721902515149]

Moist Heat or Steam Sterilization

[00721902515149]

Moist Heat or Steam Sterilization

[00721902515149]

Moist Heat or Steam Sterilization

[00721902515149]

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: 2015-07-31

On-Brand Devices [LIBERTY® Posterior Spinal System]

• 00673978039237: ROD 808-089 TSRH LIGHTLY KNURLED 6.35MM
• 00721902792694: 0 DEG ILIAC SCRW 8.5 X 90
• 00721902792687: 0 DEG ILIAC SCRW 8.5 X 80
• 00721902792670: 0 DEG ILIAC SCRW 8.5 X 70
• 00721902792663: 0 DEG ILIAC SCRW 8.5 X 100
• 00721902792656: 10 DEG OBL ILIAC SCRW 8.5 X 90
• 00721902792649: 10 DEG OBL ILIAC SCRW 8.5 X 80
• 00721902792632: 10 DEG OBL ILIAC SCRW 8.5 X 70
• 00721902792625: 10 DEG OBL ILIAC SCW 8.5 X 100
• 00721902792595: 0 DEG ILIAC SCRW 8.5 X 90
• 00721902792571: 0 DEG ILIAC SCRW 8.5 X 80
• 00721902792564: 0 DEG ILIAC SCRW 8.5 X 70
• 00721902792557: 0 DEG ILIAC SCRW 8.5 X 100
• 00721902792526: 10 DEG OBL ILIAC SCRW 8.5 X 70
• 00721902792519: 10 DEG OBL ILIAC SCRW 8.5 X 70
• 00721902792496: 10 DEG OBL ILIAC SCW 8.5 X 100
• 00721902515378: LIB 20MM CL STARC 6.35-4.5 TI
• 00721902515354: CONNECTOR X0602010 L S C S 6.35 4.5 10MM
• 00721902515323: LIB 7MM CL STARC 6.35-4.5 TI
• 00721902515149: CONNECTOR X0602030 L S C S 6.35 4.5 30MM
• 00721902512834: 10 DEG OBL ILIAC SCRW 7.5 X 70
• 00721902512827: 10 DEG OBL ILIAC SCRW 7.5 X 60
• 00721902512810: 10 DEG OBL ILIAC SCRW 7.5 X 50
• 00721902512797: 10 DEG OBL ILIAC SCRW 6.5 X 90
• 00721902512759: 10 DEG OBL ILIAC SCRW 6.5 X 50
• 00721902512742: 10 DEG OBL ILIAC SCRW 6.5 X100
• 00721902512698: 0 DEG ILIAC SCRW 7.5 X 90
• 00721902512681: 0 DEG ILIAC SCRW 7.5 X100
• 00721902512674: 0 DEG ILIAC SCRW 7.5 X100
• 00721902512667: 0 DEG ILIAC SCRW 7.5 X100
• 00721902512650: 0 DEG ILIAC SCRW 6.5 X 90
• 00721902512643: 0 DEG ILIAC SCRW 6.5 X 60
• 00721902512544: 0 DEG ILIAC SCRW 6.5 X 50
• 00721902512537: 0 DEG ILIAC SCRW 6.5 X100
• 00721902503894: 0 DEGREE ILIAC SCREW 7.5 X 90
• 00721902503863: 0 DEGREE ILIAC SCREW 7.5 X 60
• 00721902503856: 0 DEGREE ILIAC SCREW 7.5 X 50
• 00721902503849: 0 DEGREE ILIAC SCREW 7.5 X 100
• 00721902503832: 0 DEGREE ILIAC SCREW 6.5 X 90
• 00721902503801: 0 DEGREE ILIAC SCREW 6.5 X 60
• 00721902503795: 0 DEGREE ILIAC SCREW 6.5 X 50
• 00721902503696: 0 DEGREE ILIAC SCREW 6.5 X 100
• 00721902503597: OFFSET CONNECTOR FOR 5.5MM ROD
• 00721902503580: OFFSET CONNECTOR FOR 5.5MM ROD