AOS CANNULATED BLOCKING SCREW 5.0mm x 40mm

GUDID 00848665010442

ADVANCED ORTHOPEDIC SOLUTIONS INC

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

• Primary Device ID: 00848665010442
• NIH Device Record Key: 6c80c0c8-2500-414d-a3ad-e9688fe9ca6d
• Commercial Distribution Discontinuation: 2017-05-31
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: AOS CANNULATED BLOCKING SCREW 5.0mm x 40mm
• Version Model Number: S8045-040
• 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	00848665010442 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K070444

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: 2016-01-18

On-Brand Devices [AOS CANNULATED BLOCKING SCREW 5.0mm x 40mm]

• 00848665020359: 8045-040
• 00848665010442: S8045-040