EquiLOX Lumbar Expandable Cage - Bone Impactor

GUDID 00850065741079

Bone impactor

CAPTIVA SPINE, INC.

Surgical tamp, reusable

• Primary Device ID: 00850065741079
• NIH Device Record Key: 2192ee3b-e43d-4cbe-be7d-61835adb0c00
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EquiLOX Lumbar Expandable Cage - Bone Impactor
• Version Model Number: CSE06-R-0500-50
• 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: true
• 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
GS1	00850065741079 [Primary]

FDA Product Code

• LXH: Orthopedic Manual Surgical Instrument

Sterilization

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

[00850065741079]

Moist Heat or Steam Sterilization

[00850065741079]

Moist Heat or Steam Sterilization

[00850065741079]

Moist Heat or Steam Sterilization

[00850065741079]

Moist Heat or Steam Sterilization

[00850065741079]

Moist Heat or Steam Sterilization

[00850065741079]

Moist Heat or Steam Sterilization

[00850065741079]

Moist Heat or Steam Sterilization

[00850065741079]

Moist Heat or Steam Sterilization

[00850065741079]

Moist Heat or Steam Sterilization

[00850065741079]

Moist Heat or Steam Sterilization

[00850065741079]

Moist Heat or Steam Sterilization

[00850065741079]

Moist Heat or Steam Sterilization

[00850065741079]

Moist Heat or Steam Sterilization

[00850065741079]

Moist Heat or Steam Sterilization

[00850065741079]

Moist Heat or Steam Sterilization

[00850065741079]

Moist Heat or Steam Sterilization

[00850065741079]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-07-24
• Device Publish Date: 2024-07-16

On-Brand Devices [EquiLOX Lumbar Expandable Cage - Bone Impactor]

• 00850065741079: Bone impactor
• 00850065741000: Bone impactor