MAX VPC™K-WIRE DOUBLE TROCAR 233209095

GUDID 00880304812499

Biomet Orthopedics, LLC

Orthopaedic bone wire

• Primary Device ID: 00880304812499
• NIH Device Record Key: d73f24ce-0476-480e-b364-196e62a1b1cf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MAX VPC™K-WIRE DOUBLE TROCAR
• Version Model Number: 233209095
• Catalog Number: 233209095
• 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: 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(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00880304812499 [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

[00880304812499]

Moist Heat or Steam Sterilization

[00880304812499]

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: 2016-06-30

On-Brand Devices [MAX VPC™K-WIRE DOUBLE TROCAR]

• 00880304812512: 233214127
• 00880304812505: 233211105
• 00880304812499: 233209095
• 00880304812482: 133214127
• 00880304812475: 133211105
• 00880304812468: 133209095