1MM SYSTEM 01-7405

GUDID 00841036014155

BIOMET MICROFIXATION, INC

Orthopaedic bone screw, non-bioabsorbable, non-sterile

• Primary Device ID: 00841036014155
• NIH Device Record Key: 0bfacf1f-1348-4f82-8d8e-7eaae0c7f507
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 1MM SYSTEM
• Version Model Number: 01-7405
• Catalog Number: 01-7405
• Company DUNS: 046189866
• Company Name: BIOMET MICROFIXATION, 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(904)741-4400
• Email: FXJAX-ORDERS@ZIMMERBIOMET.COM
• Phone: +1(904)741-4400
• Email: FXJAX-ORDERS@ZIMMERBIOMET.COM

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841036014155 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K121589

FDA Product Code

• HBW: FASTENER, PLATE, CRANIOPLASTY

Sterilization

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

[00841036014155]

Moist Heat or Steam Sterilization

[00841036014155]

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: 2015-10-11

On-Brand Devices [1MM SYSTEM]

• 00841036014384: 01-7504
• 00841036014193: 01-7415
• 00841036014186: 01-7413
• 00841036014179: 01-7407
• 00841036014162: 01-7406
• 00841036014155: 01-7405
• 00841036014148: 01-7404
• 00841036014131: 01-7403
• 00841036014124: 01-7402
• 00841036014070: 01-7385