802503203

GUDID 00889024499461

Zimmer, Inc.

Femoral head prosthesis trial

• Primary Device ID: 00889024499461
• NIH Device Record Key: 0b46205b-c44c-443d-b4ee-cf6d3179ae69
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 802503203
• Catalog Number: 802503203
• Company DUNS: 056038268
• Company Name: Zimmer, Inc.
• 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: false
• 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)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com

Device Dimensions

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00889024499461 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K183457

FDA Product Code

• LPH: PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED

Sterilization

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

[00889024499461]

Moist Heat or Steam Sterilization

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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• 00889024684171 - SERIES A PATELLA PROTECTOR ASYMMETRIC 40MM 3PEG: 2025-01-21
• 00889024684188 - SERIES A PATELLA PROTECTOR ASYMMETRIC 34MM 3PEG: 2025-01-21
• 00889024684195 - SERIES A PATELLA PROTECTOR ASYMMETRIC 37MM 3PEG: 2025-01-21
• 00889024684201 - SERIES A PATELLA PROTECTOR ASYMMETRIC 28MM 3PEG: 2025-01-21
• 00889024684218 - SERIES A PATELLA PROTECTOR ASYMMETRIC 31MM 3PEG: 2025-01-21