PEANUT PLATING SYSTEM 24716

GUDID 00888480237303

Biomet Orthopedics, LLC

Orthopaedic bone screw, non-bioabsorbable, sterile

• Primary Device ID: 00888480237303
• NIH Device Record Key: 9201963c-beea-4341-aaeb-8e23aae3949b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PEANUT PLATING SYSTEM
• Version Model Number: 24716
• Catalog Number: 24716
• 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	00888480237303 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K070823
• Premarket Notification: K093880

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: 2015-10-24

On-Brand Devices [PEANUT PLATING SYSTEM]

• 00880304532373: 24516
• 00880304500433: 24616
• 00880304500426: 24612
• 00880304500419: 24632
• 00880304500402: 24540
• 00880304492530: 24524
• 00880304491571: 24636
• 00880304491526: 24532
• 00888480237334: 24740
• 00888480237327: 24732
• 00888480237310: 24724
• 00888480237303: 24716