K-WIRE TROCAR POINT 110008393

GUDID 70887868076939

Biomet Orthopedics, LLC

Orthopaedic bone wire

• Primary Device ID: 70887868076939
• NIH Device Record Key: 6a711587-3705-4c07-8379-65b904c7d115
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: K-WIRE TROCAR POINT
• Version Model Number: 110008393
• Catalog Number: 110008393
• Company DUNS: 129278169
• Company Name: Biomet Orthopedics, LLC
• Device Count: 6
• 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: false
• 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	00887868076930 [Primary]
GS1	70887868076939 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K140891

FDA Product Code

• HWC: Screw, fixation, bone

Sterilization

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

[70887868076939]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2024-02-19
• Device Publish Date: 2021-02-16

On-Brand Devices [K-WIRE TROCAR POINT]

• 30880304648679: IFI-491414
• 70887868076939: 110008393