Screw Caddy

GUDID M739134000907

SmartLOX Screw Caddy

CAPTIVA SPINE, INC.

Instrument tray, reusable

• Primary Device ID: M739134000907
• NIH Device Record Key: 069caa43-1634-412e-b856-ad48aa9b3f09
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Screw Caddy
• Version Model Number: 13400-0907
• 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: 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: 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	M739134000907 [Primary]

FDA Product Code

• FSM: Tray, Surgical, Instrument

Sterilization

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

[M739134000907]

Moist Heat or Steam Sterilization

[M739134000907]

Moist Heat or Steam Sterilization

[M739134000907]

Moist Heat or Steam Sterilization

[M739134000907]

Moist Heat or Steam Sterilization

[M739134000907]

Moist Heat or Steam Sterilization

[M739134000907]

Moist Heat or Steam Sterilization

[M739134000907]

Moist Heat or Steam Sterilization

[M739134000907]

Moist Heat or Steam Sterilization

[M739134000907]

Moist Heat or Steam Sterilization

[M739134000907]

Moist Heat or Steam Sterilization

[M739134000907]

Moist Heat or Steam Sterilization

[M739134000907]

Moist Heat or Steam Sterilization

[M739134000907]

Moist Heat or Steam Sterilization

[M739134000907]

Moist Heat or Steam Sterilization

[M739134000907]

Moist Heat or Steam Sterilization

[M739134000907]

Moist Heat or Steam Sterilization

[M739134000907]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-10-09
• Device Publish Date: 2023-09-29

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• 00850065741062 - EquiLOX Lumbar Expandable Cage - Bone Graft Funnel: 2024-07-24 Bone Graft Funnel
• 00850065741079 - EquiLOX Lumbar Expandable Cage - Bone Impactor: 2024-07-24 Bone impactor