Foot Extension MTIL3006002

GUDID 00841439104514

with attached Prodigy™ Lok-Bar™

MEDTEC, INC.

Indexed-immobilization patient positioning system

• Primary Device ID: 00841439104514
• NIH Device Record Key: a5eff231-9d86-40a3-a8b6-cc6377a64af3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Foot Extension
• Version Model Number: MTIL3006002
• Catalog Number: MTIL3006002
• Company DUNS: 103977526
• Company Name: MEDTEC, INC.
• Device Count: 1
• DM Exempt: true
• 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: true
• 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(712)737-8688
• Email: radiotherapy.complaints@civcort.com

Device Dimensions

• Length: 36 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841439104514 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K973842

FDA Product Code

• IXQ: Table, radiographic, stationary top

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2020-03-19
• Device Publish Date: 2017-08-02

On-Brand Devices [Foot Extension]

• 00841439104514: with attached Prodigy™ Lok-Bar™
• 00841439104507: Reusable non-sterile Interloc® foot extension with attached Interloc® Lok-Bar™