GAITWAY

GUDID 00840420169358

WRIGHT MEDICAL TECHNOLOGY, INC.

Orthopaedic bone screw, non-bioabsorbable, non-sterile

• Primary Device ID: 00840420169358
• NIH Device Record Key: e7237e13-2192-4788-9db4-e89f225dbf88
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: GAITWAY
• Version Model Number: GTW-0100
• 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
• 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 Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840420169358 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K122738

FDA Product Code

• HWC: Screw, fixation, bone

Sterilization

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

[00840420169358]

Moist Heat or Steam Sterilization

[00840420169358]

Moist Heat or Steam Sterilization

[00840420169358]

Moist Heat or Steam Sterilization

[00840420169358]

Moist Heat or Steam Sterilization

[00840420169358]

Moist Heat or Steam Sterilization

[00840420169358]

Moist Heat or Steam Sterilization

[00840420169358]

Moist Heat or Steam Sterilization

[00840420169358]

Moist Heat or Steam Sterilization

[00840420169358]

Moist Heat or Steam Sterilization

[00840420169358]

Moist Heat or Steam Sterilization

[00840420169358]

Moist Heat or Steam Sterilization

[00840420169358]

Moist Heat or Steam Sterilization

[00840420169358]

Moist Heat or Steam Sterilization

[00840420169358]

Moist Heat or Steam Sterilization

[00840420169358]

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: 2015-10-15

On-Brand Devices [GAITWAY]

• 00840420170637: 30-100-02
• 00840420169365: GTW-0115
• 00840420169358: GTW-0100
• 00840420169341: GTW-0090
• 00840420169334: GTW-0075
• 00840420169327: GTW-0065