GDLH® Posterior Spinal System

GUDID 00673978061825

ROD 855-011 5.5 MM HEX-END ROD L20 TI

MEDTRONIC SOFAMOR DANEK, INC.

Bone-screw internal spinal fixation system, non-sterile

• Primary Device ID: 00673978061825
• NIH Device Record Key: 207c8f15-14ac-4e9c-ba36-b3c659627edb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: GDLH® Posterior Spinal System
• Version Model Number: 855-011
• 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

• Outer Diameter: 5.5 Millimeter
• Outer Diameter: 5.5 Millimeter
• Outer Diameter: 5.5 Millimeter
• Outer Diameter: 5.5 Millimeter
• Length: 508 Millimeter
• Outer Diameter: 5.5 Millimeter
• Length: 508 Millimeter
• Outer Diameter: 5.5 Millimeter
• Length: 508 Millimeter
• Outer Diameter: 5.5 Millimeter
• Length: 508 Millimeter
• Outer Diameter: 5.5 Millimeter
• Length: 508 Millimeter
• Outer Diameter: 5.5 Millimeter
• Length: 508 Millimeter
• Outer Diameter: 5.5 Millimeter
• Length: 508 Millimeter
• Outer Diameter: 5.5 Millimeter
• Length: 508 Millimeter
• Outer Diameter: 5.5 Millimeter
• Length: 508 Millimeter
• Outer Diameter: 5.5 Millimeter
• Length: 508 Millimeter
• Outer Diameter: 5.5 Millimeter
• Length: 508 Millimeter
• Outer Diameter: 5.5 Millimeter
• Length: 508 Millimeter
• Outer Diameter: 5.5 Millimeter
• Length: 508 Millimeter
• Outer Diameter: 5.5 Millimeter
• Length: 508 Millimeter
• Outer Diameter: 5.5 Millimeter
• Length: 508 Millimeter
• Outer Diameter: 5.5 Millimeter
• Length: 508 Millimeter
• Outer Diameter: 5.5 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00673978061825 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K954645

FDA Product Code

• KWP: APPLIANCE, FIXATION, SPINAL INTERLAMINAL

Sterilization

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

[00673978061825]

Moist Heat or Steam Sterilization

[00673978061825]

Moist Heat or Steam Sterilization

[00673978061825]

Moist Heat or Steam Sterilization

[00673978061825]

Moist Heat or Steam Sterilization

[00673978061825]

Moist Heat or Steam Sterilization

[00673978061825]

Moist Heat or Steam Sterilization

[00673978061825]

Moist Heat or Steam Sterilization

[00673978061825]

Moist Heat or Steam Sterilization

[00673978061825]

Moist Heat or Steam Sterilization

[00673978061825]

Moist Heat or Steam Sterilization

[00673978061825]

Moist Heat or Steam Sterilization

[00673978061825]

Moist Heat or Steam Sterilization

[00673978061825]

Moist Heat or Steam Sterilization

[00673978061825]

Moist Heat or Steam Sterilization

[00673978061825]

Moist Heat or Steam Sterilization

[00673978061825]

Moist Heat or Steam Sterilization

[00673978061825]

Moist Heat or Steam Sterilization

[00673978061825]

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: 2015-08-24

On-Brand Devices [GDLH® Posterior Spinal System]

• 00673978130422: ROD 5.5X20CM HEX TI
• 00673978130415: ROD 5.5X18CM HEX SS
• 00673978130408: ROD 5.5X16CM HEX SS
• 00673978130392: ROD 5.5X14CM HEX TI
• 00673978130385: ROD 5.5X12CM HEX TI
• 00673978130361: ROD 5.5X9CM HEX TI
• 00673978130347: ROD 5.5X7CM HEX TI
• 00673978130316: ROD 5.5X4CM HEX TI
• 00673978130163: TSR TT T-BOLT 14MM 5.5 TI
• 00673978061825: ROD 855-011 5.5 MM HEX-END ROD L20 TI
• 00673978056258: ROD 845-011 5.5MM HEX END L20 51CM
• 00721902975233: ROD 5.5X30CM-TI-HEX
• 00721902975226: ROD 5.5X28CM-TI-HEX
• 00721902975219: ROD 5.5X26CM-TI-HEX
• 00721902975189: ROD 5.5X22CM-TI-HEX
• 00721902975158: ROD 5.5X11CM-TI-HEX