AOS GALILEO™ LAG SCREW 10.5mm x 120mm

GUDID 00848665004922

ADVANCED ORTHOPEDIC SOLUTIONS INC

Femur nail, sterile

• Primary Device ID: 00848665004922
• NIH Device Record Key: 68767131-706b-401c-98c5-5f41f1922466
• Commercial Distribution Discontinuation: 2017-06-09
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: AOS GALILEO™ LAG SCREW 10.5mm x 120mm
• Version Model Number: S1099-120
• Company DUNS: 117858154
• Company Name: ADVANCED ORTHOPEDIC SOLUTIONS INC
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00848665004922 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K120148

FDA Product Code

• HSB: Rod, Fixation, Intramedullary And Accessories

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-12-14

On-Brand Devices [AOS GALILEO™ LAG SCREW 10.5mm x 120mm]

• 00848665015898: 1099-120
• 00848665004922: S1099-120