AOS 13.5mm CANNULATED ENTRY REAMER

GUDID 00848665030136

ADVANCED ORTHOPEDIC SOLUTIONS INC

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• Primary Device ID: 00848665030136
• NIH Device Record Key: de325249-f12f-4d4e-84b8-befa666caa6c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AOS 13.5mm CANNULATED ENTRY REAMER
• Version Model Number: S0266
• 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

Customer Support Contacts

• Phone: 3105339966
• Email: regaffairs@aosortho.com
• Phone: 3105339966
• Email: regaffairs@aosortho.com
• Phone: 3105339966
• Email: regaffairs@aosortho.com
• Phone: 3105339966
• Email: regaffairs@aosortho.com
• Phone: 3105339966
• Email: regaffairs@aosortho.com
• Phone: 3105339966
• Email: regaffairs@aosortho.com
• Phone: 3105339966
• Email: regaffairs@aosortho.com
• Phone: 3105339966
• Email: regaffairs@aosortho.com
• Phone: 3105339966
• Email: regaffairs@aosortho.com
• Phone: 3105339966
• Email: regaffairs@aosortho.com
• Phone: 3105339966
• Email: regaffairs@aosortho.com
• Phone: 3105339966
• Email: regaffairs@aosortho.com
• Phone: 3105339966
• Email: regaffairs@aosortho.com
• Phone: 3105339966
• Email: regaffairs@aosortho.com
• Phone: 3105339966
• Email: regaffairs@aosortho.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00848665030136 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K123569

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: 2
• Public Version Date: 2020-06-08
• Device Publish Date: 2020-05-21

Devices Manufactured by ADVANCED ORTHOPEDIC SOLUTIONS INC

• 00848665027679 - COUNTERSINK: 2020-06-23
• 00848665000658 - AOS Drill, AO Style, 2.9mm x 100mm: 2020-06-08
• 00848665001235 - AOS CANCELLOUS TAP 3.5mm: 2020-06-08
• 00848665027624 - SUPRAPATELLAR TIBIAL ENTRY SHEATH: 2020-06-08
• 00848665028041 - T10 Screwdriver, Short: 2020-06-08
• 00848665028096 - 3.5mm Calibrated Drill: 2020-06-08
• 00848665028119 - AOS 2.6mm Solid Reamer: 2020-06-08
• 00848665028782 - T10 Screwdriver, Solid: 2020-06-08