SMALL DIAMETER CEMENT PLUG 414993

GUDID 00880304370470

Biomet Orthopedics, LLC

Polymer orthopaedic cement restrictor, non-bioabsorbable, sterile

• Primary Device ID: 00880304370470
• NIH Device Record Key: ff302c84-0784-4bd6-b774-a4c49275e1a9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SMALL DIAMETER CEMENT PLUG
• Version Model Number: 414993
• Catalog Number: 414993
• 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

Device Dimensions

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00880304370470 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K020045

FDA Product Code

• KWT: PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED

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 [SMALL DIAMETER CEMENT PLUG]

• 00880304370500: 414996
• 00880304370494: 414995
• 00880304370487: 414994
• 00880304370470: 414993
• 00880304370463: 414992