VHS VARI-ANGLE HIP SYSTEM 200321

GUDID 00880304279391

Biomet Orthopedics, LLC

Hip internal fixation system Hip internal fixation system

• Primary Device ID: 00880304279391
• NIH Device Record Key: b781b81f-61b1-4c3e-ae94-e72b8c40f8c1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VHS VARI-ANGLE HIP SYSTEM
• Version Model Number: 200321
• Catalog Number: 200321
• 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: 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
• 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	00880304279391 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K991806

FDA Product Code

• KTT: APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-10-24

On-Brand Devices [VHS VARI-ANGLE HIP SYSTEM]

• 00880304279414: 200328
• 00880304279407: 200325
• 00880304279391: 200321
• 00880304070943: CP253431
• 00880304070936: CP253430
• 00880304070929: CP253429