Comprehensive Anatomic Shoulder SSI004399

GUDID 00887868255809

Biomet Orthopedics, LLC

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• Primary Device ID: 00887868255809
• NIH Device Record Key: 696fdded-1126-4f90-882c-ebb20e6d2f24
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Comprehensive Anatomic Shoulder
• Version Model Number: SSI004399
• Catalog Number: SSI004399
• 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: 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) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• 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 Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887868255809 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K060694

FDA Product Code

• KWS: Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented

Sterilization

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

[00887868255809]

Moist Heat or Steam Sterilization

[00887868255809]

Moist Heat or Steam Sterilization

[00887868255809]

Moist Heat or Steam Sterilization

[00887868255809]

Moist Heat or Steam Sterilization

[00887868255809]

Moist Heat or Steam Sterilization

[00887868255809]

Moist Heat or Steam Sterilization

[00887868255809]

Moist Heat or Steam Sterilization

[00887868255809]

Moist Heat or Steam Sterilization

[00887868255809]

Moist Heat or Steam Sterilization

[00887868255809]

Moist Heat or Steam Sterilization

[00887868255809]

Moist Heat or Steam Sterilization

[00887868255809]

Moist Heat or Steam Sterilization

[00887868255809]

Moist Heat or Steam Sterilization

[00887868255809]

Moist Heat or Steam Sterilization

[00887868255809]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-08-27
• Device Publish Date: 2018-07-26

On-Brand Devices [Comprehensive Anatomic Shoulder]

• 00887868255823: SSI004595
• 00887868255816: SSI004400
• 00887868255809: SSI004399
• 00887868255793: SSI004398