K-WIRE,TROCAR POINT 2 END 35-351566

GUDID 00887868101472

Biomet Orthopedics, LLC

Orthopaedic bone wire Orthopaedic bone wire

• Primary Device ID: 00887868101472
• NIH Device Record Key: 775d1c6f-b137-4feb-a132-3b383310ee30
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: K-WIRE,TROCAR POINT 2 END
• Version Model Number: 35-351566
• Catalog Number: 35-351566
• 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	00887868101472 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K831005

FDA Product Code

• HTY: PIN, FIXATION, SMOOTH

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: 2016-09-22

On-Brand Devices [K-WIRE,TROCAR POINT 2 END]

• 00880304359642: 35-351564
• 00880304359581: 35-351534
• 00887868101489: 35-351568
• 00887868101472: 35-351566
• 00887868101458: 35-351558
• 00887868101427: 35-351538
• 00887868101380: 35-351508
• 00887868101373: 35-351504
• 00887868101335: 35-351468