LACTOSORB® 2.0MM SYSTEM 915-2024

GUDID 00841036054014

BIOMET MICROFIXATION, INC

Fluted surgical drill bit, reusable

• Primary Device ID: 00841036054014
• NIH Device Record Key: 5601327d-6b69-4b68-80c9-acf06e13355d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LACTOSORB® 2.0MM SYSTEM
• Version Model Number: 915-2024
• Catalog Number: 915-2024
• 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	00841036054014 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K062842

FDA Product Code

• HBE: DRILLS, BURRS, TREPHINES & ACCESSORIES (SIMPLE, POWERED)

Sterilization

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

[00841036054014]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-11-22
• Device Publish Date: 2015-10-11

On-Brand Devices [LACTOSORB® 2.0MM SYSTEM]

• 00841036154578: 915-1729
• 00841036150921: 915-1740
• 00841036139018: 915-1711
• 00841036126452: 915-2065
• 00841036123642: 915-1727
• 00841036122973: 915-2078
• 00841036054052: 915-2029
• 00841036054021: 915-2025
• 00841036054014: 915-2024