Kompressor™ Compression Screw System 211600

GUDID M2482116001

Kompressor™ Compression Screw System 3.5MM DRILL GUIDE

INTEGRA LIFESCIENCES CORPORATION

Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable

• Primary Device ID: M2482116001
• NIH Device Record Key: 38541622-8aa2-4a5f-a4ae-678e37ad0d5a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Kompressor™ Compression Screw System
• Version Model Number: 211600
• Catalog Number: 211600
• Company DUNS: 963856096
• Company Name: INTEGRA LIFESCIENCES CORPORATION
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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

Customer Support Contacts

• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
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• Device Size Text, specify: 0
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• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	10381780280057 [Primary]
HIBCC	M2482116001 [Secondary]

FDA Product Code

• FZX: Guide, surgical, instrument

Sterilization

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

[M2482116001]

Moist Heat or Steam Sterilization

[M2482116001]

Moist Heat or Steam Sterilization

[M2482116001]

Moist Heat or Steam Sterilization

[M2482116001]

Moist Heat or Steam Sterilization

[M2482116001]

Moist Heat or Steam Sterilization

[M2482116001]

Moist Heat or Steam Sterilization

[M2482116001]

Moist Heat or Steam Sterilization

[M2482116001]

Moist Heat or Steam Sterilization

[M2482116001]

Moist Heat or Steam Sterilization

[M2482116001]

Moist Heat or Steam Sterilization

[M2482116001]

Moist Heat or Steam Sterilization

[M2482116001]

Moist Heat or Steam Sterilization

[M2482116001]

Moist Heat or Steam Sterilization

[M2482116001]

Moist Heat or Steam Sterilization

[M2482116001]

Moist Heat or Steam Sterilization

[M2482116001]

Moist Heat or Steam Sterilization

[M2482116001]

Moist Heat or Steam Sterilization

[M2482116001]

Moist Heat or Steam Sterilization

[M2482116001]

Moist Heat or Steam Sterilization

[M2482116001]

Moist Heat or Steam Sterilization

[M2482116001]

Moist Heat or Steam Sterilization

[M2482116001]

Moist Heat or Steam Sterilization

[M2482116001]

Moist Heat or Steam Sterilization

[M2482116001]

Moist Heat or Steam Sterilization

[M2482116001]

Moist Heat or Steam Sterilization

[M2482116001]

Moist Heat or Steam Sterilization

[M2482116001]

Moist Heat or Steam Sterilization

[M2482116001]

Moist Heat or Steam Sterilization

[M2482116001]

Moist Heat or Steam Sterilization

[M2482116001]

Moist Heat or Steam Sterilization

[M2482116001]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2020-04-06
• Device Publish Date: 2018-04-13

On-Brand Devices [Kompressor™ Compression Screw System]

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• M2482116101: Kompressor™ Compression Screw System 2.8MM DRILL GUIDE
• M2482116011: Kompressor™ Compression Screw System 2.5MM DRILL GUIDE
• M2482116001: Kompressor™ Compression Screw System 3.5MM DRILL GUIDE
• M2482150011: KOMPRESSOR STERILIZATION TRAY
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• M2482103181: The mini Kompressor Compression Screw is a two-piece fixation device intended for the use in the