Activmotion ATGP2-ST

GUDID 03700569602499

NEWCLIP TECHNICS

Orthopaedic fixation plate, non-bioabsorbable

• Primary Device ID: 03700569602499
• NIH Device Record Key: 39559ef1-0585-487c-ace3-45318d7644b6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Activmotion
• Version Model Number: ATGP2-ST
• Catalog Number: ATGP2-ST
• Company DUNS: 263281904
• Company Name: NEWCLIP TECHNICS
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	03700569602499 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K173746

FDA Product Code

• HRS: Plate, Fixation, Bone

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-11-21
• Device Publish Date: 2024-11-13

On-Brand Devices [Activmotion]

• 03700569627669: ATGP2
• 03700569627652: ATDP2
• 03700569617608: ATGP1
• 03700569617592: ATDP1
• 03700569602499: ATGP2-ST
• 03700569602475: ATDP2-ST