Rampart-O 270-0010

GUDID M7402700010

Distractor Paddle, 10 mm

SPINEOLOGY INC.

Surgical implant template, reusable

• Primary Device ID: M7402700010
• NIH Device Record Key: 4fe14392-c995-4ab9-95a3-4d49dc21184e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Rampart-O
• Version Model Number: 83-05-01-10
• Catalog Number: 270-0010
• 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 Dimensions

• Height: 10 Millimeter
• Height: 10 Millimeter
• Height: 10 Millimeter
• Height: 10 Millimeter
• Height: 10 Millimeter
• Height: 10 Millimeter
• Height: 10 Millimeter
• Height: 10 Millimeter
• Height: 10 Millimeter
• Height: 10 Millimeter
• Height: 10 Millimeter
• Height: 10 Millimeter
• Height: 10 Millimeter
• Height: 10 Millimeter
• Height: 10 Millimeter
• Height: 10 Millimeter
• Height: 10 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	M7402700010 [Primary]

FDA Product Code

• LXH: Orthopedic Manual Surgical Instrument

Sterilization

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

[M7402700010]

Moist Heat or Steam Sterilization

[M7402700010]

Moist Heat or Steam Sterilization

[M7402700010]

Moist Heat or Steam Sterilization

[M7402700010]

Moist Heat or Steam Sterilization

[M7402700010]

Moist Heat or Steam Sterilization

[M7402700010]

Moist Heat or Steam Sterilization

[M7402700010]

Moist Heat or Steam Sterilization

[M7402700010]

Moist Heat or Steam Sterilization

[M7402700010]

Moist Heat or Steam Sterilization

[M7402700010]

Moist Heat or Steam Sterilization

[M7402700010]

Moist Heat or Steam Sterilization

[M7402700010]

Moist Heat or Steam Sterilization

[M7402700010]

Moist Heat or Steam Sterilization

[M7402700010]

Moist Heat or Steam Sterilization

[M7402700010]

Moist Heat or Steam Sterilization

[M7402700010]

Moist Heat or Steam Sterilization

[M7402700010]

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 [Rampart-O]

• M7402700013: Distractor Paddle, 13 mm
• M7402700012: Distractor Paddle, 12 mm
• M7402700011: Distractor Paddle, 11 mm
• M7402700010: Distractor Paddle, 10 mm
• M7402700009: Distractor Paddle, 9 mm
• M7402700008: Distractor Paddle, 8 mm
• M7402700007: Distractor Paddle, 7 mm
• M7402700016: Distractor Paddle, 16 mm
• M7402700015: Distractor Paddle, 15 mm
• M7402700014: Distractor Paddle, 14 mm
• M7402500041: Rampart Remover
• M7402700021: Slap Mallet Extension