JUGGERKNOT SOFT ANCHORS 110005307

GUDID 00880304568198

Biomet Sports Medicine, LLC

Suturing unit, single-use

• Primary Device ID: 00880304568198
• NIH Device Record Key: 9cf33be9-e02e-4d97-bc88-94b75a4eb459
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: JUGGERKNOT SOFT ANCHORS
• Version Model Number: 110005307
• Catalog Number: 110005307
• Company DUNS: 627100159
• Company Name: Biomet Sports Medicine, 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	00880304568198 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K110145

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: 2020-02-06
• Device Publish Date: 2015-10-24

On-Brand Devices [JUGGERKNOT SOFT ANCHORS]

• 00880304568228: 110005320
• 00880304568211: 110005319
• 00880304568204: 110005315
• 00880304568198: 110005307
• 00880304548114: 110005241
• 00880304548107: 110005242
• 00880304548091: 110005096
• 00880304548084: 110005093
• 00880304545854: 010000324
• 00880304543416: 916030
• 00880304543409: 912075
• 00880304522350: 912029
• 00880304511699: 912069
• 00880304509627: 912031
• 00880304508590: 912050
• 00880304477315: 912000
• 00880304477193: 912030