THP™ HIP FRACTURE PLATING SYSTEMHIP FRACTURE PLATE 14-451102

GUDID 00887868164378

Biomet Orthopedics, LLC

Hip internal fixation system

• Primary Device ID: 00887868164378
• NIH Device Record Key: 6f023491-4dd9-45fd-aeb1-8a3346bd524a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: THP™ HIP FRACTURE PLATING SYSTEMHIP FRACTURE PLATE
• Version Model Number: 14-451102
• Catalog Number: 14-451102
• 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

Device Dimensions

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887868164378 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K140018

FDA Product Code

• JDO: DEVICE, FIXATION, PROXIMAL FEMORAL, IMPLANT

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: 2017-12-29

On-Brand Devices [THP™ HIP FRACTURE PLATING SYSTEMHIP FRACTURE PLATE]

• 00887868164385: 14-451104
• 00887868164378: 14-451102
• 00887868164293: 14-451004
• 00887868164286: 14-451002