TOGGLELOC WITH ZIPLOOP 110017308

GUDID 00880304676947

Biomet Sports Medicine, LLC

Tendon/ligament bone anchor, non-bioabsorbable

• Primary Device ID: 00880304676947
• NIH Device Record Key: 939a6117-9a1e-4131-b2bd-7c26f1cf1bbb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TOGGLELOC WITH ZIPLOOP
• Version Model Number: 110017308
• Catalog Number: 110017308
• Company DUNS: 627100159
• Company Name: Biomet Sports Medicine, 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	00880304676947 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K141263

FDA Product Code

• JDR: STAPLE, FIXATION, BONE

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: 2015-11-03

On-Brand Devices [TOGGLELOC WITH ZIPLOOP]

• 00880304676947: 110017308
• 00880304478923: 909874
• 00880304472709: 909849
• 00880304464773: 909848