Genesis I XK000733-4

GUDID 00885556915219

GENESIS ARTICULAR INSERT LARGE RIGHT 8MM

Smith & Nephew, Inc.

Uncoated knee tibia prosthesis, polyethylene Uncoated knee tibia prosthesis, polyethylene Uncoated knee tibia prosthesis, polyethylene Uncoated knee tibia prosthesis, polyethylene Uncoated knee tibia prosthesis, polyethylene Uncoated knee tibia prosthesis, polyethylene Uncoated knee tibia prosthesis, polyethylene Uncoated knee tibia prosthesis, polyethylene Uncoated knee tibia prosthesis, polyethylene Uncoated knee tibia prosthesis, polyethylene Uncoated knee tibia prosthesis, polyethylene Uncoated knee tibia prosthesis, polyethylene Uncoated knee tibia prosthesis, polyethylene Uncoated knee tibia prosthesis, polyethylene Uncoated knee tibia prosthesis, polyethylene Uncoated knee tibia prosthesis, polyethylene Uncoated knee tibia prosthesis, polyethylene Uncoated knee tibia prosthesis, polyethylene

• Primary Device ID: 00885556915219
• NIH Device Record Key: 1034e7e9-ec0c-4c20-a9e3-c14e5d43d1f1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Genesis I
• Version Model Number: XK000733-4
• Catalog Number: XK000733-4
• Company DUNS: 045483575
• Company Name: Smith & Nephew, 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)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM

Device Identifiers

Device Issuing Agency	Device ID
GS1	00885556915219 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K871146

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: 2024-01-30
• Device Publish Date: 2024-01-22

On-Brand Devices [Genesis I]

• 00885556914076: GENESIS ARTICULAR INSERT LARGE RIGHT 10MM
• 00885556914069: GENESIS ARTICULAR INSERT MEDIUM LEFT 10MM
• 00885556915219: GENESIS ARTICULAR INSERT LARGE RIGHT 8MM
• 00885556915202: GENESIS ARTICULAR INSERT MEDIUM LEFT 12MM