3595-6-090

GUDID 07613327084139

Steinmann Pin, Diamond Point, both ends

Stryker Trauma SA

Orthopaedic bone wire

• Primary Device ID: 07613327084139
• NIH Device Record Key: 9faf69ef-7fa2-43c0-921e-f170f8d15794
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 3595-6-090
• Catalog Number: 3595-6-090
• Company DUNS: 481999654
• Company Name: Stryker Trauma SA
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• 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

Device Dimensions

• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0
• Length: 230 Millimeter
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327084139 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K211508

FDA Product Code

• HTY: PIN, FIXATION, SMOOTH
• JDW: Pin, Fixation, Threaded

Sterilization

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

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

[07613327084139]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-10-25
• Device Publish Date: 2018-09-24

Devices Manufactured by Stryker Trauma SA

• 07613327555554 - VARIAX: 2024-10-30 T-handle, Cannulated Three-jaw Chuck
• 07613327605808 - PANGEA: 2024-10-18 Small Frag. Proximal Tibia Targeter Tray
• 07613327603101 - REUNION: 2024-10-09 Modular Glenoid Surface Trial
• 07613327603118 - REUNION: 2024-10-09 Modular Glenoid Surface Trial
• 07613327603125 - REUNION: 2024-10-09 Modular Glenoid Surface Trial
• 07613327603132 - REUNION: 2024-10-09 Modular Humeral Head Trial
• 07613327603149 - REUNION: 2024-10-09 Modular Glenoid Surface Trial
• 07613327603156 - REUNION: 2024-10-09 Modular Humeral Head Trial