Long Cannulated Screw System

GUDID 00840420119070

WRIGHT MEDICAL TECHNOLOGY, INC.

Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile

• Primary Device ID: 00840420119070
• NIH Device Record Key: 1c05bbdc-bffa-453a-baf8-5311b50030ec
• Commercial Distribution Discontinuation: 2015-11-20
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Long Cannulated Screw System
• Version Model Number: 10-250
• 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: 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)238-7117
• 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
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com

Device Dimensions

• Outer Diameter: 7.5 Millimeter
• Length: 50 Millimeter
• Outer Diameter: 7.5 Millimeter
• Length: 50 Millimeter
• Outer Diameter: 7.5 Millimeter
• Length: 50 Millimeter
• Outer Diameter: 7.5 Millimeter
• Length: 50 Millimeter
• Outer Diameter: 7.5 Millimeter
• Length: 50 Millimeter
• Outer Diameter: 7.5 Millimeter
• Length: 50 Millimeter
• Outer Diameter: 7.5 Millimeter
• Length: 50 Millimeter
• Outer Diameter: 7.5 Millimeter
• Length: 50 Millimeter
• Outer Diameter: 7.5 Millimeter
• Length: 50 Millimeter
• Outer Diameter: 7.5 Millimeter
• Length: 50 Millimeter
• Outer Diameter: 7.5 Millimeter
• Length: 50 Millimeter
• Outer Diameter: 7.5 Millimeter
• Length: 50 Millimeter
• Outer Diameter: 7.5 Millimeter
• Length: 50 Millimeter
• Outer Diameter: 7.5 Millimeter
• Length: 50 Millimeter
• Outer Diameter: 7.5 Millimeter
• Length: 50 Millimeter
• Outer Diameter: 7.5 Millimeter
• Length: 50 Millimeter
• Outer Diameter: 7.5 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840420119070 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K042310

FDA Product Code

• HWC: Screw, fixation, bone

Sterilization

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

[00840420119070]

Moist Heat or Steam Sterilization

[00840420119070]

Moist Heat or Steam Sterilization

[00840420119070]

Moist Heat or Steam Sterilization

[00840420119070]

Moist Heat or Steam Sterilization

[00840420119070]

Moist Heat or Steam Sterilization

[00840420119070]

Moist Heat or Steam Sterilization

[00840420119070]

Moist Heat or Steam Sterilization

[00840420119070]

Moist Heat or Steam Sterilization

[00840420119070]

Moist Heat or Steam Sterilization

[00840420119070]

Moist Heat or Steam Sterilization

[00840420119070]

Moist Heat or Steam Sterilization

[00840420119070]

Moist Heat or Steam Sterilization

[00840420119070]

Moist Heat or Steam Sterilization

[00840420119070]

Moist Heat or Steam Sterilization

[00840420119070]

Moist Heat or Steam Sterilization

[00840420119070]

Moist Heat or Steam Sterilization

[00840420119070]

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 [Long Cannulated Screw System]

• 00840420119247: RETIRED
• 00840420119230: RETIRED
• 00840420119223: RETIRED
• 00840420119216: RETIRED
• 00840420119209: RETIRED
• 00840420119193: RETIRED
• 00840420119186: RETIRED
• 00840420119179: 10-280
• 00840420119162: 10-260
• 00840420119155: 10-180
• 00840420119148: 10-160
• 00840420119131: RETIRED
• 00840420119124: RETIRED
• 00840420119117: RETIRED
• 00840420119100: RETIRED
• 00840420119094: 10-165
• 00840420119087: RETIRED
• 00840420119070: 10-250
• 00840420119063: RETIRED