JuggerKnotless® 110017436

GUDID 00880304672635

Biomet Orthopedics, LLC

Surgical drill guide, reusable

• Primary Device ID: 00880304672635
• NIH Device Record Key: dc452141-247c-4215-9255-dce648abc930
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: JuggerKnotless®
• Version Model Number: 110017436
• Catalog Number: 110017436
• 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	00880304672635 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K123485

FDA Product Code

• MBI: Fastener, fixation, nondegradable, soft tissue

Sterilization

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

[00880304672635]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-03-24
• Device Publish Date: 2020-03-16

On-Brand Devices [JuggerKnotless®]

• 00880304673649: 110003172
• 00880304672659: 110003182
• 00880304672642: 110003181
• 00880304672673: 110017433
• 00880304672666: 110017434
• 00880304672635: 110017436
• 00887868462986: 110005201