CANNULATED SCREW 3.0MM X 40MM (PARTIAL THREAD) 110009789

GUDID 00887868110023

Biomet Orthopedics, LLC

Orthopaedic bone screw, non-bioabsorbable, sterile

• Primary Device ID: 00887868110023
• NIH Device Record Key: f6778ee4-5062-41da-b60b-74a45e08a076
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CANNULATED SCREW 3.0MM X 40MM (PARTIAL THREAD)
• Version Model Number: 110009789
• Catalog Number: 110009789
• 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	00887868110023 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K143188

FDA Product Code

• HWC: Screw, 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: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-26

On-Brand Devices [CANNULATED SCREW 3.0MM X 40MM (PARTIAL THREAD)]

• 00887868110023: 110009789
• 00887868107092: 110007522