AOS SET SCREW, A/R

GUDID 00848665013832

ADVANCED ORTHOPEDIC SOLUTIONS INC

Bone nail end-cap, sterile

• Primary Device ID: 00848665013832
• NIH Device Record Key: a4cae763-c95e-4528-a410-0fc0c41e0f91
• Commercial Distribution Discontinuation: 2017-06-27
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: AOS SET SCREW, A/R
• Version Model Number: S1085
• 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	00848665013832 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K021008

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: 4
• Public Version Date: 2018-10-22
• Device Publish Date: 2015-12-04

On-Brand Devices [AOS SET SCREW, A/R ]

• 00848665015652: 1085
• 00848665013832: S1085