Cannulated Screw System NK 0030-27

GUDID 04042409431265

K-wire with trocar point, ø3.0, L 270

aap Implantate AG

Orthopaedic bone wire Orthopaedic bone wire

• Primary Device ID: 04042409431265
• NIH Device Record Key: a44ec479-aaca-420d-87b7-42b74f675ef1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Cannulated Screw System
• Version Model Number: NK 0030-27
• Catalog Number: NK 0030-27
• Company DUNS: 328420633
• Company Name: aap Implantate AG
• Device Count: 10
• DM Exempt: true
• 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: true
• Expiration Date: false
• 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	04042409175848 [Primary]
GS1	04042409431265 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K131459

FDA Product Code

• HTY: Pin, Fixation, Smooth

Sterilization

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

[04042409431265]

Moist Heat or Steam Sterilization

[04042409431265]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-06-29
• Device Publish Date: 2020-06-19

On-Brand Devices [Cannulated Screw System]

• 04042409431265: K-wire with trocar point, ø3.0, L 270
• 04042409431289: K-wire with trocar point, ø2.5, L 270