MAX VPC™ 231201430

GUDID 00887868337475

Biomet Orthopedics, LLC

Surgical drill guide, reusable

• Primary Device ID: 00887868337475
• NIH Device Record Key: 6243cb03-125c-48a7-9770-74d5227d1369
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MAX VPC™
• Version Model Number: 231201430
• Catalog Number: 231201430
• 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: 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(800)348-9500
• Email: customerservice@zimmerbiomet.com

Device Dimensions

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887868337475 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K160058

FDA Product Code

• HWC: Screw, fixation, bone

Sterilization

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

[00887868337475]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-09-30
• Device Publish Date: 2019-09-20

On-Brand Devices [MAX VPC™]

• 00887868337482: 231201440
• 00887868337475: 231201430
• 00887868337468: 231201425
• 00887868445255: 133214127
• 00887868445248: 133211105
• 00887868445231: 133209095