Uni Femoral Knee WZ-1-1003

GUDID B046WZ110030

Uni Femoral Knee Size 3

SIGNAL MEDICAL CORPORATION

Coated knee femur prosthesis Coated knee femur prosthesis

• Primary Device ID: B046WZ110030
• NIH Device Record Key: 6a8769cd-619a-4f44-a7b4-36966d96bbfe
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Uni Femoral Knee
• Version Model Number: 3
• Catalog Number: WZ-1-1003
• Company DUNS: 169289308
• Company Name: SIGNAL MEDICAL CORPORATION
• 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: true
• 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

Customer Support Contacts

• Phone: 8103647070
• Email: jgorney@signalmd.com
• Phone: 8103647070
• Email: jgorney@signalmd.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B046WZ110030 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K012800

FDA Product Code

• HRY: Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, 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: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-08-05

On-Brand Devices [Uni Femoral Knee]

• B046WZ110050: Uni Femoral Knee Size 5
• B046WZ110040: Uni Femoral Knee Size 4
• B046WZ110030: Uni Femoral Knee Size 3
• B046WZ110020: Uni Femoral Knee Size 2