OPTILOCK PLATING SYSTEM 26766

GUDID 00888480249269

Biomet Orthopedics, LLC

Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile

• Primary Device ID: 00888480249269
• NIH Device Record Key: 450d8c47-a8f8-4001-bdea-a3dc195cc6c0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: OPTILOCK PLATING SYSTEM
• Version Model Number: 26766
• Catalog Number: 26766
• 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: 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
• 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	00888480249269 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K061098

FDA Product Code

• HRS: PLATE, FIXATION, BONE

Sterilization

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

[00888480249269]

Moist Heat or Steam Sterilization

[00888480249269]

Moist Heat or Steam Sterilization

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 [OPTILOCK PLATING SYSTEM]

• 00880304510883: 27114
• 00880304510876: 27112
• 00888480251552: 27110
• 00888480249269: 26766