FasTouch™ FTP25

GUDID 07290017155104

FasTouch™ Permanent Fixation System 25 Permanent Fasteners

VIA SURGICAL LTD

Soft-tissue/mesh anchor, non-bioabsorbable

• Primary Device ID: 07290017155104
• NIH Device Record Key: 385a1ff0-f1e3-423d-a9e2-038459ea90e2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FasTouch™
• Version Model Number: FTP25
• Catalog Number: FTP25
• Company DUNS: 600319250
• Company Name: VIA SURGICAL LTD
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +18009696331
• Email: CS@progressivemedinc.com

Device Dimensions

• Length: 37 Centimeter
• Length: 37 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290017155104 [Primary]
GS1	17290017155101 [Package]; Package: Box [5 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K162252

FDA Product Code

• GDW: Staple, Implantable

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2020-05-06
• Device Publish Date: 2017-08-21

On-Brand Devices [FasTouch™]

• 17290017155118: FasTouch™ Permanent Reloadable Cartridge 10 Permanent Fasteners
• 07290017155104: FasTouch™ Permanent Fixation System 25 Permanent Fasteners
• 17290017155040: Sterile Sample of the FasTouch™ Permanent Reloadable Cartridge 10 Permanent Fasteners
• 17290017155019: Sterile Sample of the FasTouch™ Permanent Fixation System 25 Permanent Fasteners