4-Hole Drill Guide

GUDID M739203000200N0

4-Hole Drill Guide for NAV

CAPTIVA SPINE, INC.

Surgical drill guide, reusable

• Primary Device ID: M739203000200N0
• NIH Device Record Key: a03d314c-4f20-4f56-8454-2af0b401ca57
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 4-Hole Drill Guide
• Version Model Number: 20300-0200N
• Company DUNS: 836975784
• Company Name: CAPTIVA SPINE, INC.
• 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: 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: 561-277-9480
• Email: info@captivaspine.com
• Phone: 561-277-9480
• Email: info@captivaspine.com
• Phone: 561-277-9480
• Email: info@captivaspine.com
• Phone: 561-277-9480
• Email: info@captivaspine.com
• Phone: 561-277-9480
• Email: info@captivaspine.com
• Phone: 561-277-9480
• Email: info@captivaspine.com
• Phone: 561-277-9480
• Email: info@captivaspine.com
• Phone: 561-277-9480
• Email: info@captivaspine.com
• Phone: 561-277-9480
• Email: info@captivaspine.com
• Phone: 561-277-9480
• Email: info@captivaspine.com
• Phone: 561-277-9480
• Email: info@captivaspine.com
• Phone: 561-277-9480
• Email: info@captivaspine.com
• Phone: 561-277-9480
• Email: info@captivaspine.com
• Phone: 561-277-9480
• Email: info@captivaspine.com
• Phone: 561-277-9480
• Email: info@captivaspine.com
• Phone: 561-277-9480
• Email: info@captivaspine.com
• Phone: 561-277-9480
• Email: info@captivaspine.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	M739203000200N0 [Primary]

FDA Product Code

• HXY: Brace, Drill

Sterilization

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

[M739203000200N0]

Moist Heat or Steam Sterilization

[M739203000200N0]

Moist Heat or Steam Sterilization

[M739203000200N0]

Moist Heat or Steam Sterilization

[M739203000200N0]

Moist Heat or Steam Sterilization

[M739203000200N0]

Moist Heat or Steam Sterilization

[M739203000200N0]

Moist Heat or Steam Sterilization

[M739203000200N0]

Moist Heat or Steam Sterilization

[M739203000200N0]

Moist Heat or Steam Sterilization

[M739203000200N0]

Moist Heat or Steam Sterilization

[M739203000200N0]

Moist Heat or Steam Sterilization

[M739203000200N0]

Moist Heat or Steam Sterilization

[M739203000200N0]

Moist Heat or Steam Sterilization

[M739203000200N0]

Moist Heat or Steam Sterilization

[M739203000200N0]

Moist Heat or Steam Sterilization

[M739203000200N0]

Moist Heat or Steam Sterilization

[M739203000200N0]

Moist Heat or Steam Sterilization

[M739203000200N0]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-01-22
• Device Publish Date: 2024-01-12

On-Brand Devices [4-Hole Drill Guide]

• M7392030002000: 20300-0200
• M739203000200N0: 4-Hole Drill Guide for NAV
• M739203000210: 4-Hole LD Drill Guide