CLAW

GUDID 00840420109651

WRIGHT MEDICAL TECHNOLOGY, INC.

Orthopaedic fixation plate, non-bioabsorbable, non-sterile

• Primary Device ID: 00840420109651
• NIH Device Record Key: 61caf176-f8d7-479e-842f-38e34b8f0b3b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CLAW
• Version Model Number: 40120015
• 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	00840420109651 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K133715

FDA Product Code

• HRS: PLATE, FIXATION, BONE

Sterilization

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

[00840420109651]

Moist Heat or Steam Sterilization

[00840420109651]

Moist Heat or Steam Sterilization

[00840420109651]

Moist Heat or Steam Sterilization

[00840420109651]

Moist Heat or Steam Sterilization

[00840420109651]

Moist Heat or Steam Sterilization

[00840420109651]

Moist Heat or Steam Sterilization

[00840420109651]

Moist Heat or Steam Sterilization

[00840420109651]

Moist Heat or Steam Sterilization

[00840420109651]

Moist Heat or Steam Sterilization

[00840420109651]

Moist Heat or Steam Sterilization

[00840420109651]

Moist Heat or Steam Sterilization

[00840420109651]

Moist Heat or Steam Sterilization

[00840420109651]

Moist Heat or Steam Sterilization

[00840420109651]

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 [CLAW]

• 00889797009423: 40120031
• 00840420109675: 40120025
• 00840420109668: 40120020
• 00840420109651: 40120015
• 00889797009546: 40130010