Nano fx® FURS-0100

GUDID M528FURS01000

NanoFx, Thumble

ARTHROSURFACE INCORPORATED

Subchondral bone needling device lever, single-use

• Primary Device ID: M528FURS01000
• NIH Device Record Key: 64885158-4901-48f7-bc9b-4d4ce0b31b7c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Nano fx®
• Version Model Number: FURS-0100
• Catalog Number: FURS-0100
• Company DUNS: 144666109
• Company Name: ARTHROSURFACE INCORPORATED
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• 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: 508-520-3003
• Email: contact@arthrosurface.com
• Phone: 508-520-3003
• Email: contact@arthrosurface.com
• Phone: 508-520-3003
• Email: contact@arthrosurface.com
• Phone: 508-520-3003
• Email: contact@arthrosurface.com
• Phone: 508-520-3003
• Email: contact@arthrosurface.com
• Phone: 508-520-3003
• Email: contact@arthrosurface.com
• Phone: 508-520-3003
• Email: contact@arthrosurface.com
• Phone: 508-520-3003
• Email: contact@arthrosurface.com
• Phone: 508-520-3003
• Email: contact@arthrosurface.com
• Phone: 508-520-3003
• Email: contact@arthrosurface.com
• Phone: 508-520-3003
• Email: contact@arthrosurface.com
• Phone: 508-520-3003
• Email: contact@arthrosurface.com
• Phone: 508-520-3003
• Email: contact@arthrosurface.com
• Phone: 508-520-3003
• Email: contact@arthrosurface.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	M528FURS01000 [Primary]

FDA Product Code

• LXH: Orthopedic Manual Surgical Instrument

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2021-04-07
• Device Publish Date: 2015-10-20

Devices Manufactured by ARTHROSURFACE INCORPORATED

• M5288RC150080 - RevoMotion: 2024-04-22
• M5288RG232000 - RevoMotion: 2024-04-22 Glenosphere, 32mm, +2 Lateral Offset
• M5288RS210200 - RevoMotion: 2024-04-22 Center Screw, Ø 6.5mm x 20mm
• M5288RS210250 - RevoMotion: 2024-04-22
• M5288RS210300 - RevoMotion: 2024-04-22
• M5288RS210350 - RevoMotion: 2024-04-22
• M5288RS210400 - RevoMotion: 2024-04-22
• M5288RS210450 - RevoMotion: 2024-04-22