MAX VPC™CANNULATED DRIVER HEX AO 212001230

GUDID 00880304814264

Biomet Orthopedics, LLC

Surgical screwdriver, reusable

• Primary Device ID: 00880304814264
• NIH Device Record Key: bfca66b6-80bc-4694-9d2d-d75bd50b254c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MAX VPC™CANNULATED DRIVER HEX AO
• Version Model Number: 212001230
• Catalog Number: 212001230
• Company DUNS: 129278169
• Company Name: Biomet Orthopedics, LLC
• 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: false
• 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: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com

Device Dimensions

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00880304814264 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K160058

FDA Product Code

• HWC: Screw, fixation, bone

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2018-10-05
• Device Publish Date: 2016-09-26

On-Brand Devices [MAX VPC™CANNULATED DRIVER HEX AO]

• 00880304814271: 212001240
• 00880304814264: 212001230
• 00880304814257: 212001225