OSS FEMORAL AUGMENT TRIAL 110018749

GUDID 00880304679344

Biomet Orthopedics, LLC

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• Primary Device ID: 00880304679344
• NIH Device Record Key: 73ae44a1-1941-44b6-80ef-28e69d51c002
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: OSS FEMORAL AUGMENT TRIAL
• Version Model Number: 110018749
• Catalog Number: 110018749
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• 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 Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00880304679344 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K141331

FDA Product Code

• KRO: PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER

Sterilization

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

[00880304679344]

Moist Heat or Steam Sterilization

[00880304679344]

Moist Heat or Steam Sterilization

[00880304679344]

Moist Heat or Steam Sterilization

[00880304679344]

Moist Heat or Steam Sterilization

[00880304679344]

Moist Heat or Steam Sterilization

[00880304679344]

Moist Heat or Steam Sterilization

[00880304679344]

Moist Heat or Steam Sterilization

[00880304679344]

Moist Heat or Steam Sterilization

[00880304679344]

Moist Heat or Steam Sterilization

[00880304679344]

Moist Heat or Steam Sterilization

[00880304679344]

Moist Heat or Steam Sterilization

[00880304679344]

Moist Heat or Steam Sterilization

[00880304679344]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-02-07
• Device Publish Date: 2016-10-27

On-Brand Devices [OSS FEMORAL AUGMENT TRIAL]

• 00880304679344: 110018749
• 00880304679337: 110018748