00-5220-034-04

GUDID 00889024187313

Zimmer, Inc.

Tibial insert

• Primary Device ID: 00889024187313
• NIH Device Record Key: 7aa14ccc-6d6b-4ab9-a344-9c9e8a9d84cb
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 5220-34-04
• Catalog Number: 00-5220-034-04
• 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: 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

• Height: 15 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00889024187313 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K830121

FDA Product Code

• JWH: PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-07-31
• Device Publish Date: 2015-09-24

Devices Manufactured by Zimmer, Inc.

• 00889024691759 - PSN TASP PROV BTM R CD +3MM: 2025-05-26
• 00889024691766 - PSN TASP PROV BTM R GH +3MM: 2025-05-26
• 00889024691773 - PSN TASP PROV BTM L J +3MM: 2025-05-26
• 00889024691780 - PSN TASP PROV BTM R J +3MM: 2025-05-26
• 00889024691797 - PSN TASP PROV BTM L GH +3MM: 2025-05-26
• 00889024691803 - PSN TASP PROV BTM L CD +3MM: 2025-05-26
• 00889024691810 - PSN TASP PROV BTM R EF +3MM: 2025-05-26
• 00889024691827 - PSN TASP PROV BTM L EF +3MM: 2025-05-26