CAPTURE Facet Screw Set System 430-0029

GUDID M7404300029

EMG Cannula

SPINEOLOGY INC.

Laparoscopic access cannula dilator

• Primary Device ID: M7404300029
• NIH Device Record Key: 982c0be5-3250-48bc-aa33-71e3305a3e85
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CAPTURE Facet Screw Set System
• Version Model Number: 70-02-019
• Catalog Number: 430-0029
• Company DUNS: 033014361
• Company Name: SPINEOLOGY INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• 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: 651-256-8500
• Email: info@spineology.com
• Phone: 651-256-8500
• Email: info@spineology.com
• Phone: 651-256-8500
• Email: info@spineology.com
• Phone: 651-256-8500
• Email: info@spineology.com
• Phone: 651-256-8500
• Email: info@spineology.com
• Phone: 651-256-8500
• Email: info@spineology.com
• Phone: 651-256-8500
• Email: info@spineology.com
• Phone: 651-256-8500
• Email: info@spineology.com
• Phone: 651-256-8500
• Email: info@spineology.com
• Phone: 651-256-8500
• Email: info@spineology.com
• Phone: 651-256-8500
• Email: info@spineology.com
• Phone: 651-256-8500
• Email: info@spineology.com
• Phone: 651-256-8500
• Email: info@spineology.com
• Phone: 651-256-8500
• Email: info@spineology.com
• Phone: 651-256-8500
• Email: info@spineology.com
• Phone: 651-256-8500
• Email: info@spineology.com
• Phone: 651-256-8500
• Email: info@spineology.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	M7404300029 [Primary]

FDA Product Code

• LXH: Orthopedic Manual Surgical Instrument

Sterilization

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

[M7404300029]

Moist Heat or Steam Sterilization

[M7404300029]

Moist Heat or Steam Sterilization

[M7404300029]

Moist Heat or Steam Sterilization

[M7404300029]

Moist Heat or Steam Sterilization

[M7404300029]

Moist Heat or Steam Sterilization

[M7404300029]

Moist Heat or Steam Sterilization

[M7404300029]

Moist Heat or Steam Sterilization

[M7404300029]

Moist Heat or Steam Sterilization

[M7404300029]

Moist Heat or Steam Sterilization

[M7404300029]

Moist Heat or Steam Sterilization

[M7404300029]

Moist Heat or Steam Sterilization

[M7404300029]

Moist Heat or Steam Sterilization

[M7404300029]

Moist Heat or Steam Sterilization

[M7404300029]

Moist Heat or Steam Sterilization

[M7404300029]

Moist Heat or Steam Sterilization

[M7404300029]

Moist Heat or Steam Sterilization

[M7404300029]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-06-10
• Device Publish Date: 2024-05-31

On-Brand Devices [CAPTURE Facet Screw Set System]

• M7404300032: Graft Spacer
• M7404300031: Rasp
• M7404300030: Dilator
• M7404300029: EMG Cannula
• M7404300028: Screw Remover
• M7404300027: Cannula cleaner
• M7404300026: Driver Cannula
• M7404300025: Driver Shaft
• M7404300024: Tap
• M7404300023: Drill Guide
• M7403150015: Capture Drill
• M7404300038: Palm Ratchet Handle