Perimeter Interbody Fusion

GUDID 00613994989956

PERIMETER 3499001 INSERTER INNER SHAFT

MEDTRONIC SOFAMOR DANEK, INC.

Orthopaedic implant inserter/extractor, reusable

• Primary Device ID: 00613994989956
• NIH Device Record Key: 5ed03311-0cfd-4848-85f8-e5df60e369c8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Perimeter Interbody Fusion
• Version Model Number: 3499001
• 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: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00613994989956 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K113642

FDA Product Code

• MAX: Intervertebral fusion device with bone graft, lumbar

Sterilization

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

[00613994989956]

Moist Heat or Steam Sterilization

[00613994989956]

Moist Heat or Steam Sterilization

[00613994989956]

Moist Heat or Steam Sterilization

[00613994989956]

Moist Heat or Steam Sterilization

[00613994989956]

Moist Heat or Steam Sterilization

[00613994989956]

Moist Heat or Steam Sterilization

[00613994989956]

Moist Heat or Steam Sterilization

[00613994989956]

Moist Heat or Steam Sterilization

[00613994989956]

Moist Heat or Steam Sterilization

[00613994989956]

Moist Heat or Steam Sterilization

[00613994989956]

Moist Heat or Steam Sterilization

[00613994989956]

Moist Heat or Steam Sterilization

[00613994989956]

Moist Heat or Steam Sterilization

[00613994989956]

Moist Heat or Steam Sterilization

[00613994989956]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2019-04-23
• Device Publish Date: 2015-09-10

On-Brand Devices [Perimeter Interbody Fusion]

• 00613994989963: PERIMETER 3499002 INSERTER OUTER SLEEVE
• 00613994989956: PERIMETER 3499001 INSERTER INNER SHAFT