TUNNELOC® 906512

GUDID 00887868226649

Biomet Orthopedics, LLC

Tendon/ligament bone anchor, non-bioabsorbable

• Primary Device ID: 00887868226649
• NIH Device Record Key: 80b46af1-7a35-4b54-a4f8-f8d99e6ce41e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TUNNELOC®
• Version Model Number: 906512
• Catalog Number: 906512
• Company DUNS: 129278169
• Company Name: Biomet Orthopedics, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• 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	00887868226649 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K103145

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: 2017-10-09

On-Brand Devices [TUNNELOC®]

• 00887868226670: 906515
• 00887868226663: 906514
• 00887868226656: 906513
• 00887868226649: 906512