802202801

GUDID 00889024498778

Zimmer, Inc.

Metallic femoral head prosthesis

• Primary Device ID: 00889024498778
• NIH Device Record Key: 073a10d2-c673-407f-9824-ee4dd4d03edb
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 802202801
• Catalog Number: 802202801
• Company DUNS: 056038268
• Company Name: Zimmer, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• 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)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com

Device Dimensions

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00889024498778 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K183457

FDA Product Code

• KWY: Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-03-27
• Device Publish Date: 2020-03-19

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• 00889024658196 - Persona® Knee System: 2025-02-14
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