02226010

GUDID H679022260100

3.0MM HEADLESS COMPRESSION SCREW-SHORT THREAD 10MM

Synthes GmbH

Orthopaedic bone screw, non-bioabsorbable, non-sterile

• Primary Device ID: H679022260100
• NIH Device Record Key: dc6d8f04-6887-4920-9a1e-6f9b2e80fcae
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 02.226.010
• Catalog Number: 02226010
• Company DUNS: 486711679
• Company Name: Synthes GmbH
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	10886982057662 [Primary]
HIBCC	H679022260100 [Secondary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K050636

FDA Product Code

• HWC: Screw, fixation, bone

Sterilization

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

[H679022260100]

Moist Heat or Steam Sterilization

[H679022260100]

Moist Heat or Steam Sterilization

[H679022260100]

Moist Heat or Steam Sterilization

[H679022260100]

Moist Heat or Steam Sterilization

[H679022260100]

Moist Heat or Steam Sterilization

[H679022260100]

Moist Heat or Steam Sterilization

[H679022260100]

Moist Heat or Steam Sterilization

[H679022260100]

Moist Heat or Steam Sterilization

[H679022260100]

Moist Heat or Steam Sterilization

[H679022260100]

Moist Heat or Steam Sterilization

[H679022260100]

Moist Heat or Steam Sterilization

[H679022260100]

Moist Heat or Steam Sterilization

[H679022260100]

Moist Heat or Steam Sterilization

[H679022260100]

Moist Heat or Steam Sterilization

[H679022260100]

Moist Heat or Steam Sterilization

[H679022260100]

Moist Heat or Steam Sterilization

[H679022260100]

Moist Heat or Steam Sterilization

[H679022260100]

Moist Heat or Steam Sterilization

[H679022260100]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2022-05-27
• Device Publish Date: 2015-09-14

Devices Manufactured by Synthes GmbH

• 07612334270139 - EXPert Nail: 2025-10-02 TRAY F/TIBIAL NAIL EX SP INSTR
• H679310930 - NA: 2025-10-01 SMALL CHUCK WITH KEY
• 10886982350190 - NA: 2025-09-22 2.0MM STRAIGHT PLATE 20 HOLES
• 10887587078465 - NA: 2025-09-19 NONRETAINING SCREWDRIVER BLADE FOR 90DEG SCREWDRIVER
• 10886982349873 - NA: 2025-09-01 CANNULATED CIRCULAR REAMER 16MM
• 10886982349880 - NA: 2025-09-01 CANNULATED CIRCULAR REAMER 18MM
• 10886982349897 - NA: 2025-09-01 CANNULATED CIRCULAR REAMER 20MM
• 10886982349903 - NA: 2025-09-01 CANNULATED CIRCULAR REAMER 22MM