EZLOC™ 904777

GUDID 00880304992245

Biomet Orthopedics, LLC

Tendon/ligament bone anchor, non-bioabsorbable

• Primary Device ID: 00880304992245
• NIH Device Record Key: fb8b9dd5-8a5e-4264-a458-1c2be427f6cb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EZLOC™
• Version Model Number: 904777
• Catalog Number: 904777
• 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

Device Dimensions

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00880304992245 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K053461

FDA Product Code

• MBI: Fastener, fixation, nondegradable, soft tissue

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: 2019-03-21
• Device Publish Date: 2017-07-28

On-Brand Devices [EZLOC™]

• 00880304992269: 904779
• 00880304992252: 904778
• 00880304992245: 904777
• 00887868511127: 904763
• 00887868511110: 904762
• 00887868556654: 904764
• 00887868567544: 904761