3813-3-090S

GUDID 07613154711246

Stryker Trauma SA

Orthopaedic bone wire

• Primary Device ID: 07613154711246
• NIH Device Record Key: 03bfe97d-705c-41cf-8a0e-720b8780a68f
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 3813-3-090S
• Catalog Number: 3813-3-090S
• 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: 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613154711246 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K211508

FDA Product Code

• JDW: PIN, FIXATION, THREADED

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-08-22
• Device Publish Date: 2023-08-14

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