AOS FRACTURE REDUCTION SCREW HUMERAL NAIL

GUDID 00848665017014

ADVANCED ORTHOPEDIC SOLUTIONS INC

Humerus nail, non-sterile

• Primary Device ID: 00848665017014
• NIH Device Record Key: 78f69460-83e8-44b3-969f-3e67a98d60a1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AOS FRACTURE REDUCTION SCREW HUMERAL NAIL
• Version Model Number: 1175
• 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	00848665017014 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K090478

FDA Product Code

• HSB: Rod, Fixation, Intramedullary And Accessories

Sterilization

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

[00848665017014]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-10-27

On-Brand Devices [AOS FRACTURE REDUCTION SCREW HUMERAL NAIL]

• 00848665017014: 1175
• 00848665005745: S1175