BePOD® Cannulated Arthrodesis Screws

GUDID 03661489684319

FOURNITURES HOSPITALIERES INDUSTRIE

Orthopaedic bone screw, non-bioabsorbable, sterile

• Primary Device ID: 03661489684319
• NIH Device Record Key: 049c6b66-1461-4bfe-af4c-1b93ca339bee
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BePOD® Cannulated Arthrodesis Screws
• Version Model Number: 268431 - BEPOD CANNULATED ARTHRODESIS SCREW L30MM
• Company DUNS: 261839898
• Company Name: FOURNITURES HOSPITALIERES INDUSTRIE
• 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: 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	03661489684319 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K170040

FDA Product Code

• HWC: Screw, Fixation, Bone

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: 2024-02-19
• Device Publish Date: 2017-04-19

On-Brand Devices [BePOD® Cannulated Arthrodesis Screws]

• 03661489684364: 268436 - BEPOD CANNULATED ARTHRODESIS SCREW L40MM
• 03661489684357: 268435 - BEPOD CANNULATED ARTHRODESIS SCREW L38MM
• 03661489684340: 268434 - BEPOD CANNULATED ARTHRODESIS SCREW L36MM
• 03661489684333: 268433 - BEPOD CANNULATED ARTHRODESIS SCREW L34MM
• 03661489684326: 268432 - BEPOD CANNULATED ARTHRODESIS SCREW L32MM
• 03661489684319: 268431 - BEPOD CANNULATED ARTHRODESIS SCREW L30MM
• 03661489684302: 268430 - BEPOD CANNULATED ARTHRODESIS SCREW L28MM