Kompressor™

GUDID M248KOMPSET1

Kompressor™ Instrument Set (21-5000)

Ascension Orthopedics, Inc.

Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile

• Primary Device ID: M248KOMPSET1
• NIH Device Record Key: 8c76ab0e-f5fa-4fb2-be54-cecbdb631a00
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Kompressor™
• Version Model Number: KOMPSET
• Company DUNS: 942377524
• Company Name: Ascension Orthopedics, Inc.
• 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: false
• Lot Batch: false
• Serial Number: true
• 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

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	10381780257271 [Primary]
HIBCC	M248KOMPSET1 [Secondary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K040356

FDA Product Code

• HWC: Screw, fixation, bone

Sterilization

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

[M248KOMPSET1]

Moist Heat or Steam Sterilization

[M248KOMPSET1]

Moist Heat or Steam Sterilization

[M248KOMPSET1]

Moist Heat or Steam Sterilization

[M248KOMPSET1]

Moist Heat or Steam Sterilization

[M248KOMPSET1]

Moist Heat or Steam Sterilization

[M248KOMPSET1]

Moist Heat or Steam Sterilization

[M248KOMPSET1]

Moist Heat or Steam Sterilization

[M248KOMPSET1]

Moist Heat or Steam Sterilization

[M248KOMPSET1]

Moist Heat or Steam Sterilization

[M248KOMPSET1]

Moist Heat or Steam Sterilization

[M248KOMPSET1]

Moist Heat or Steam Sterilization

[M248KOMPSET1]

Moist Heat or Steam Sterilization

[M248KOMPSET1]

Moist Heat or Steam Sterilization

[M248KOMPSET1]

Moist Heat or Steam Sterilization

[M248KOMPSET1]

Moist Heat or Steam Sterilization

[M248KOMPSET1]

Moist Heat or Steam Sterilization

[M248KOMPSET1]

Moist Heat or Steam Sterilization

[M248KOMPSET1]

Moist Heat or Steam Sterilization

[M248KOMPSET1]

Moist Heat or Steam Sterilization

[M248KOMPSET1]

Moist Heat or Steam Sterilization

[M248KOMPSET1]

Moist Heat or Steam Sterilization

[M248KOMPSET1]

Moist Heat or Steam Sterilization

[M248KOMPSET1]

Moist Heat or Steam Sterilization

[M248KOMPSET1]

Moist Heat or Steam Sterilization

[M248KOMPSET1]

Moist Heat or Steam Sterilization

[M248KOMPSET1]

Moist Heat or Steam Sterilization

[M248KOMPSET1]

Moist Heat or Steam Sterilization

[M248KOMPSET1]

Moist Heat or Steam Sterilization

[M248KOMPSET1]

Moist Heat or Steam Sterilization

[M248KOMPSET1]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2021-03-04
• Device Publish Date: 2016-07-25

Devices Manufactured by Ascension Orthopedics, Inc.

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• 10381780123033 - CAPTURE™ High Torque Screw System: 2023-09-18 The washer is used in conjunction with the Capture High Torque Screw System.
• 10381780123040 - CAPTURE™ High Torque Screw System: 2023-09-18 The washer is used in conjunction with the Capture High Torque Screw System.
• 10381780123057 - CAPTURE™ High Torque Screw System: 2023-09-18 The washer is used in conjunction with the Capture High Torque Screw System.
• 10381780123064 - CAPTURE™ High Torque Screw System: 2023-09-18 The washer is used in conjunction with the Capture High Torque Screw System.
• M26922286111 - Integra®: 2023-09-18 Integra® Total Foot System K-Wire is used for temporary fixation.