4.0mm x 32mm Gridlock Ankle Screw

GUDID 00812926025902

TRILLIANT SURGICAL, LTD.

Orthopaedic bone screw, non-bioabsorbable, non-sterile

• Primary Device ID: 00812926025902
• NIH Device Record Key: 460e2e4e-c85c-4b68-8405-d6333376125d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 4.0mm x 32mm Gridlock Ankle Screw
• Version Model Number: 304-40-032
• Company DUNS: 828829072
• Company Name: TRILLIANT SURGICAL, LTD.
• 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: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Dimensions

• Length: 32 Millimeter
• Length: 32 Millimeter
• Length: 32 Millimeter
• Length: 32 Millimeter
• Outer Diameter: 4 Millimeter
• Length: 32 Millimeter
• Outer Diameter: 4 Millimeter
• Length: 32 Millimeter
• Outer Diameter: 4 Millimeter
• Length: 32 Millimeter
• Outer Diameter: 4 Millimeter
• Length: 32 Millimeter
• Outer Diameter: 4 Millimeter
• Length: 32 Millimeter
• Outer Diameter: 4 Millimeter
• Length: 32 Millimeter
• Outer Diameter: 4 Millimeter
• Length: 32 Millimeter
• Outer Diameter: 4 Millimeter
• Length: 32 Millimeter
• Outer Diameter: 4 Millimeter
• Length: 32 Millimeter
• Outer Diameter: 4 Millimeter
• Length: 32 Millimeter
• Outer Diameter: 4 Millimeter
• Length: 32 Millimeter
• Outer Diameter: 4 Millimeter
• Length: 32 Millimeter
• Outer Diameter: 4 Millimeter
• Length: 32 Millimeter
• Outer Diameter: 4 Millimeter
• Length: 32 Millimeter
• Outer Diameter: 4 Millimeter
• Length: 32 Millimeter
• Outer Diameter: 4 Millimeter
• Length: 32 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00812926025902 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K160177

FDA Product Code

• HWC: Screw, Fixation, Bone

Sterilization

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

[00812926025902]

Moist Heat or Steam Sterilization

[00812926025902]

Moist Heat or Steam Sterilization

[00812926025902]

Moist Heat or Steam Sterilization

[00812926025902]

Moist Heat or Steam Sterilization

[00812926025902]

Moist Heat or Steam Sterilization

[00812926025902]

Moist Heat or Steam Sterilization

[00812926025902]

Moist Heat or Steam Sterilization

[00812926025902]

Moist Heat or Steam Sterilization

[00812926025902]

Moist Heat or Steam Sterilization

[00812926025902]

Moist Heat or Steam Sterilization

[00812926025902]

Moist Heat or Steam Sterilization

[00812926025902]

Moist Heat or Steam Sterilization

[00812926025902]

Moist Heat or Steam Sterilization

[00812926025902]

Moist Heat or Steam Sterilization

[00812926025902]

Moist Heat or Steam Sterilization

[00812926025902]

Moist Heat or Steam Sterilization

[00812926025902]

Moist Heat or Steam Sterilization

[00812926025902]

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: 2017-03-02

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