OrthoSolutions 'System26' Bone Screws OS900030-NS

GUDID 05055662956030

K-WIRE FOR 4.0MM SCREW DRILL TIP THREADED TIP 1.6 X 150MM

ORTHO SOLUTIONS HOLDINGS LIMITED

Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire

• Primary Device ID: 05055662956030
• NIH Device Record Key: 903771fb-db11-4a9d-a982-e771b75ddf51
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: OrthoSolutions 'System26' Bone Screws
• Version Model Number: OS900030-NS
• Catalog Number: OS900030-NS
• Company DUNS: 218648211
• Company Name: ORTHO SOLUTIONS HOLDINGS LIMITED
• 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: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +441621843599
• Email: quality@orthosol.com
• Phone: +441621843599
• Email: quality@orthosol.com
• Phone: +441621843599
• Email: quality@orthosol.com
• Phone: +441621843599
• Email: quality@orthosol.com
• Phone: +441621843599
• Email: quality@orthosol.com
• Phone: +441621843599
• Email: quality@orthosol.com
• Phone: +441621843599
• Email: quality@orthosol.com
• Phone: +441621843599
• Email: quality@orthosol.com
• Phone: +441621843599
• Email: quality@orthosol.com
• Phone: +441621843599
• Email: quality@orthosol.com
• Phone: +441621843599
• Email: quality@orthosol.com
• Phone: +441621843599
• Email: quality@orthosol.com
• Phone: +441621843599
• Email: quality@orthosol.com
• Phone: +441621843599
• Email: quality@orthosol.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	05055662956030 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K163489

FDA Product Code

• HTY: Pin, Fixation, Smooth

Sterilization

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

[05055662956030]

Moist Heat or Steam Sterilization

[05055662956030]

Moist Heat or Steam Sterilization

[05055662956030]

Moist Heat or Steam Sterilization

[05055662956030]

Moist Heat or Steam Sterilization

[05055662956030]

Moist Heat or Steam Sterilization

[05055662956030]

Moist Heat or Steam Sterilization

[05055662956030]

Moist Heat or Steam Sterilization

[05055662956030]

Moist Heat or Steam Sterilization

[05055662956030]

Moist Heat or Steam Sterilization

[05055662956030]

Moist Heat or Steam Sterilization

[05055662956030]

Moist Heat or Steam Sterilization

[05055662956030]

Moist Heat or Steam Sterilization

[05055662956030]

Moist Heat or Steam Sterilization

[05055662956030]

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: 2017-03-16