Freedom® 802403201

GUDID 00889024499027

Zimmer, Inc.

Metallic femoral head prosthesis

• Primary Device ID: 00889024499027
• NIH Device Record Key: a98bba95-c435-4e84-8bb0-6e3422c38392
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Freedom®
• Version Model Number: 802403201
• Catalog Number: 802403201
• 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	00889024499027 [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: 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

On-Brand Devices [Freedom®]

• 00889024499119: 802403606
• 00889024499102: 802403605
• 00889024499096: 802403604
• 00889024499089: 802403603
• 00889024499072: 802403602
• 00889024499065: 802403601
• 00889024499058: 802403204
• 00889024499041: 802403203
• 00889024499034: 802403202
• 00889024499027: 802403201