Mega Fix 2870720T

GUDID 04048551112649

Megafix-T titanium interference Screw, 7 x 20 mm

Karl Storz GmbH & Co. KG

Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile

• Primary Device ID: 04048551112649
• NIH Device Record Key: d03d533c-0b1b-4508-b274-41f566de2b99
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Mega Fix
• Version Model Number: 2870720T
• Catalog Number: 2870720T
• Company DUNS: 315731430
• Company Name: Karl Storz GmbH & Co. KG
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• 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: true
• 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: +14242188201
• Email: regulatory@karlstorz.com
• Phone: +14242188201
• Email: regulatory@karlstorz.com
• Phone: +14242188201
• Email: regulatory@karlstorz.com
• Phone: +14242188201
• Email: regulatory@karlstorz.com
• Phone: +14242188201
• Email: regulatory@karlstorz.com
• Phone: +14242188201
• Email: regulatory@karlstorz.com
• Phone: +14242188201
• Email: regulatory@karlstorz.com
• Phone: +14242188201
• Email: regulatory@karlstorz.com
• Phone: +14242188201
• Email: regulatory@karlstorz.com
• Phone: +14242188201
• Email: regulatory@karlstorz.com
• Phone: +14242188201
• Email: regulatory@karlstorz.com
• Phone: +14242188201
• Email: regulatory@karlstorz.com
• Phone: +14242188201
• Email: regulatory@karlstorz.com
• Phone: +14242188201
• Email: regulatory@karlstorz.com
• Phone: +14242188201
• Email: regulatory@karlstorz.com
• Phone: +14242188201
• Email: regulatory@karlstorz.com
• Phone: +14242188201
• Email: regulatory@karlstorz.com

Device Dimensions

• Width: 7 Millimeter
• Length: 20 Millimeter
• Width: 7 Millimeter
• Length: 20 Millimeter
• Width: 7 Millimeter
• Length: 20 Millimeter
• Width: 7 Millimeter
• Length: 20 Millimeter
• Width: 7 Millimeter
• Length: 20 Millimeter
• Width: 7 Millimeter
• Length: 20 Millimeter
• Width: 7 Millimeter
• Length: 20 Millimeter
• Width: 7 Millimeter
• Length: 20 Millimeter
• Width: 7 Millimeter
• Length: 20 Millimeter
• Width: 7 Millimeter
• Length: 20 Millimeter
• Width: 7 Millimeter
• Length: 20 Millimeter
• Width: 7 Millimeter
• Length: 20 Millimeter
• Width: 7 Millimeter
• Length: 20 Millimeter
• Width: 7 Millimeter
• Length: 20 Millimeter
• Width: 7 Millimeter
• Length: 20 Millimeter
• Width: 7 Millimeter
• Length: 20 Millimeter
• Width: 7 Millimeter
• Length: 20 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	04048551112649 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K030368

FDA Product Code

• HWC: Screw, Fixation, Bone

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2022-02-21
• Device Publish Date: 2015-10-09

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