"2.7MM" SYSTEM 91-2720

GUDID 00888233011945

BIOMET MICROFIXATION, INC

Orthopaedic bone screw, non-bioabsorbable, non-sterile

• Primary Device ID: 00888233011945
• NIH Device Record Key: 1fd67841-a550-427b-9f38-a0f33fa32ef9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: "2.7MM" SYSTEM
• Version Model Number: 91-2720
• Catalog Number: 91-2720
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00888233011945 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K001238

FDA Product Code

• JEY: PLATE, BONE

Sterilization

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

[00888233011945]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2024-02-19
• Device Publish Date: 2020-06-18

On-Brand Devices ["2.7MM" SYSTEM]

• 00841036152796: 91-2720
• 00841036065645: 99-9958
• 00888233011945: 91-2720