CAPTURE 420-5340

GUDID M7404205340

Capture Facet Screw

SPINEOLOGY INC.

Spinal bone screw, non-bioabsorbable

• Primary Device ID: M7404205340
• NIH Device Record Key: 319e2a44-59cf-4001-a5c6-f5c8e9e93993
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CAPTURE
• Version Model Number: 70-01-001-4
• Catalog Number: 420-5340
• Company DUNS: 033014361
• Company Name: SPINEOLOGY INC.
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• 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: +1(612)256-8500
• Email: info@spineology.com
• Phone: +1(612)256-8500
• Email: info@spineology.com
• Phone: +1(612)256-8500
• Email: info@spineology.com
• Phone: +1(612)256-8500
• Email: info@spineology.com
• Phone: +1(612)256-8500
• Email: info@spineology.com
• Phone: +1(612)256-8500
• Email: info@spineology.com
• Phone: +1(612)256-8500
• Email: info@spineology.com
• Phone: +1(612)256-8500
• Email: info@spineology.com
• Phone: +1(612)256-8500
• Email: info@spineology.com
• Phone: +1(612)256-8500
• Email: info@spineology.com
• Phone: +1(612)256-8500
• Email: info@spineology.com
• Phone: +1(612)256-8500
• Email: info@spineology.com
• Phone: +1(612)256-8500
• Email: info@spineology.com
• Phone: +1(612)256-8500
• Email: info@spineology.com
• Phone: +1(612)256-8500
• Email: info@spineology.com
• Phone: +1(612)256-8500
• Email: info@spineology.com
• Phone: +1(612)256-8500
• Email: info@spineology.com

Device Dimensions

• Length: 40 Millimeter
• Device Size Text, specify: 0
• Length: 40 Millimeter
• Device Size Text, specify: 0
• Length: 40 Millimeter
• Device Size Text, specify: 0
• Length: 40 Millimeter
• Device Size Text, specify: 0
• Length: 40 Millimeter
• Device Size Text, specify: 0
• Length: 40 Millimeter
• Device Size Text, specify: 0
• Length: 40 Millimeter
• Device Size Text, specify: 0
• Length: 40 Millimeter
• Device Size Text, specify: 0
• Length: 40 Millimeter
• Device Size Text, specify: 0
• Length: 40 Millimeter
• Device Size Text, specify: 0
• Length: 40 Millimeter
• Device Size Text, specify: 0
• Length: 40 Millimeter
• Device Size Text, specify: 0
• Length: 40 Millimeter
• Device Size Text, specify: 0
• Length: 40 Millimeter
• Device Size Text, specify: 0
• Length: 40 Millimeter
• Device Size Text, specify: 0
• Length: 40 Millimeter
• Device Size Text, specify: 0
• Length: 40 Millimeter
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	M7404205340 [Primary]

FDA Product Code

• MNH: Orthosis, spondylolisthesis spinal fixation

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2024-07-23
• Device Publish Date: 2015-10-05

On-Brand Devices [CAPTURE]

• M7404205350: Capture Facet Screw
• M7404205345: Capture Facet Screw
• M7404205340: Capture Facet Screw
• M7404205335: Capture Facet Screw
• M7404205330: Capture Facet Screw
• M7404205325: Capture Facet Screw
• M7404205320: Capture Facet Screw
• M7404105350: Capture Facet Screw
• M7404105345: Capture Facet Screw
• M7404105340: Capture Facet Screw
• M7404105335: Capture Facet Screw
• M7404105330: Capture Facet Screw
• M7404105325: Capture Facet Screw