5 MM BONE SCREW X 22 MM

GUDID M209216020

BIOPRO, INC.

Orthopaedic bone screw, non-bioabsorbable, sterile

• Primary Device ID: M209216020
• NIH Device Record Key: 39466d2c-ef63-48b9-a122-903ab73834cb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 5 MM BONE SCREW X 22 MM
• Version Model Number: 21602
• Company DUNS: 618749857
• Company Name: BIOPRO, 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: 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
HIBCC	M209216020 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K163627

FDA Product Code

• HWC: Screw, 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: 2019-06-20
• Device Publish Date: 2019-06-12

On-Brand Devices [5 MM BONE SCREW X 22 MM ]

• M209216120: 21612
• M209216020: 21602