Snapshot™ Fixation System 110018166

GUDID 00887868251054

Biomet Orthopedics, LLC

Ligament bone anchor

• Primary Device ID: 00887868251054
• NIH Device Record Key: 24f8d47f-13a1-4a4f-9adc-4e8f3a467b47
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Snapshot™ Fixation System
• Version Model Number: 110018166
• Catalog Number: 110018166
• 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: 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 Identifiers

Device Issuing Agency	Device ID
GS1	00887868251054 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K143037

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: 2
• Public Version Date: 2019-01-08
• Device Publish Date: 2018-09-14

On-Brand Devices [Snapshot™ Fixation System]

• 00880304685512: 110019010
• 00887868251061: 110019010
• 00887868251054: 110018166