5150-9-960

GUDID 07613327093308

Sterile Wrist Kit

Stryker Trauma SA

General internal orthopaedic fixation system implantation kit

• Primary Device ID: 07613327093308
• NIH Device Record Key: 6774ea17-07bf-4e72-9554-b4e8a4f1ad43
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 5150-9-960
• Catalog Number: 5150-9-960
• Company DUNS: 481999654
• Company Name: Stryker Trauma SA
• 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327093308 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K001886

FDA Product Code

• JDW: PIN, FIXATION, THREADED

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-09-24

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• 07613327603132 - REUNION: 2024-10-09 Modular Humeral Head Trial
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• 07613327603156 - REUNION: 2024-10-09 Modular Humeral Head Trial