TAPERLOC COMPLETE XR 123 FEMORAL 51-102070

GUDID 00880304516908

Biomet Orthopedics, LLC

Coated hip femur prosthesis, modular

• Primary Device ID: 00880304516908
• NIH Device Record Key: 617b6f24-6293-445f-8b39-2a6fd0f7ff88
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TAPERLOC COMPLETE XR 123 FEMORAL
• Version Model Number: 51-102070
• Catalog Number: 51-102070
• 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
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00880304516908 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K120030

FDA Product Code

• KWL: Prosthesis, hip, hemi-, femoral, metal

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-10-24

On-Brand Devices [TAPERLOC COMPLETE XR 123 FEMORAL]

• 00880304517196: 51-105180
• 00880304517189: 51-105170
• 00880304517172: 51-105160
• 00880304517165: 51-105150
• 00880304517158: 51-105140
• 00880304517141: 51-105130
• 00880304517134: 51-105120
• 00880304517127: 51-105110
• 00880304517110: 51-105100
• 00880304517103: 51-105090
• 00880304516915: 51-102080
• 00880304516908: 51-102070
• 00880304516892: 51-102060
• 00880304516885: 51-102050
• 00880304516878: 51-102040
• 00880304517226: 51-105240
• 00880304517219: 51-105220
• 00880304517202: 51-105200