Finn® Knee System 180031

GUDID 00887868251672

Biomet Orthopedics, LLC

Knee stem

• Primary Device ID: 00887868251672
• NIH Device Record Key: aa1db304-80fc-48e1-baf5-d319f3da8b1b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Finn® Knee System
• Version Model Number: 180031
• Catalog Number: 180031
• 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 Dimensions

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887868251672 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K974558

FDA Product Code

• KRO: PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-07-06
• Device Publish Date: 2018-05-29

On-Brand Devices [Finn® Knee System]

• 00887868251764: 180042
• 00887868251757: 180041
• 00887868251740: 180040
• 00887868251733: 180038
• 00887868251726: 180037
• 00887868251719: 180036
• 00887868251702: 180035
• 00887868251696: 180033
• 00887868251689: 180032
• 00887868251672: 180031
• 00887868251665: 180030
• 00887868251658: 180029
• 00887868251641: 180028