MINI HARPOON 902923

GUDID 00880304404663

Biomet Sports Medicine, LLC

Tendon/ligament bone anchor, non-bioabsorbable

• Primary Device ID: 00880304404663
• NIH Device Record Key: 56f90b40-5ddc-4b2d-9d24-49cca98218ef
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MINI HARPOON
• Version Model Number: 902923
• Catalog Number: 902923
• 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	00880304404663 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K943806

FDA Product Code

• HWC: Screw, 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: 2015-10-24

On-Brand Devices [MINI HARPOON]

• 00880304464810: 902941
• 00880304404663: 902923
• 00880304000674: 902922