GUDID 00840420124500

WRIGHT MEDICAL TECHNOLOGY, INC.

Orthopaedic bone washer, non-sterile

• Primary Device ID: 00840420124500
• NIH Device Record Key: feb277f9-efef-429d-988d-4548b27c5431
• Commercial Distribution Discontinuation: 2016-01-13
• Commercial Distribution Status: Not in Commercial Distribution
• Version Model Number: 5881003540
• Company DUNS: 807201207
• Company Name: WRIGHT MEDICAL TECHNOLOGY, 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: true
• Expiration Date: false
• 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)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840420124500 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K091243

FDA Product Code

• HRS: PLATE, FIXATION, BONE

Sterilization

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

[00840420124500]

Moist Heat or Steam Sterilization

[00840420124500]

Moist Heat or Steam Sterilization

[00840420124500]

Moist Heat or Steam Sterilization

[00840420124500]

Moist Heat or Steam Sterilization

[00840420124500]

Moist Heat or Steam Sterilization

[00840420124500]

Moist Heat or Steam Sterilization

[00840420124500]

Moist Heat or Steam Sterilization

[00840420124500]

Moist Heat or Steam Sterilization

[00840420124500]

Moist Heat or Steam Sterilization

[00840420124500]

Moist Heat or Steam Sterilization

[00840420124500]

Moist Heat or Steam Sterilization

[00840420124500]

Moist Heat or Steam Sterilization

[00840420124500]

Moist Heat or Steam Sterilization

[00840420124500]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-10-01

Devices Manufactured by WRIGHT MEDICAL TECHNOLOGY, INC.

• 00889797104579 - N/A: 2024-12-03 Screwdriver
• 00889797104159 - N/A: 2024-10-21 Procedure Pack Sterile
• 00889797109802 - N/A: 2024-10-15 SOLO™ Proximal Guide Block
• 00889797109819 - N/A: 2024-10-15 SOLO™ Corner Removal Guide
• 00889797103923 - PROstep MIS: 2024-09-23 Chamfer Screw
• 00889797106351 - Made-To-Order: 2024-09-11 Swanson Toe Grommet Seater
• 00889797107433 - Made-To-Order: 2024-09-11 Inbone® Strike Rod
• 00889797107457 - Made-To-Order: 2024-09-11 Inbone® Strike Rod