World Knee CR TiN Femur Right

GUDID 09348215105747

SIGNATURE ORTHOPAEDICS PTY LTD

Coated knee femur prosthesis

• Primary Device ID: 09348215105747
• NIH Device Record Key: d736ee03-26d7-4a4e-a859-de613d5c0c18
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: World Knee CR TiN Femur Right
• Version Model Number: 121-20-4312
• Company DUNS: 751993028
• Company Name: SIGNATURE ORTHOPAEDICS PTY LTD
• 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	09348215105747 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K223062

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: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-03-08
• Device Publish Date: 2023-02-28

On-Brand Devices [World Knee CR TiN Femur Right]

• 09348215106102: 121-20-4912
• 09348215106041: 121-20-4812
• 09348215105983: 121-20-4712
• 09348215105921: 121-20-4612
• 09348215105860: 121-20-4512
• 09348215105808: 121-20-4412
• 09348215105747: 121-20-4312
• 09348215105686: 121-20-4212
• 09348215105624: 121-20-4112