ANSWER HIP SYSTEM 162501

GUDID 00880304252660

Biomet Orthopedics, LLC

Uncoated femoral stem prosthesis, one-piece

• Primary Device ID: 00880304252660
• NIH Device Record Key: 9db6cfe5-fd48-47e5-8626-a15870e217db
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ANSWER HIP SYSTEM
• Version Model Number: 162501
• Catalog Number: 162501
• 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	00880304252660 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K931194

FDA Product Code

• JDG: Prosthesis, hip, femoral component, cemented, 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 [ANSWER HIP SYSTEM]

• 00880304252820: 162605
• 00880304252776: 162601
• 00880304252714: 162505
• 00880304252707: 162504
• 00880304252684: 162503
• 00880304252660: 162501
• 00880304010604: 162502
• 00880304009158: 162604
• 00880304005365: 162602
• 00880304001947: 162603