Fibulink FGS-1100

GUDID 00863176000317

AKROS MEDICAL INC

Tendon/ligament bone anchor, non-bioabsorbable

• Primary Device ID: 00863176000317
• NIH Device Record Key: 4e43c1b5-5d5b-4036-a6ca-309af98d31c2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Fibulink
• Version Model Number: FGS-1100
• Catalog Number: FGS-1100
• Company DUNS: 053433644
• Company Name: AKROS MEDICAL INC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• Human Cell/Tissue Product: false
• Device Kit: true
• 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 1 800-255-2500
• Email: xx@xx.xx
• Phone: 1 800-255-2500
• Email: xx@xx.xx
• Phone: 1 800-255-2500
• Email: xx@xx.xx
• Phone: 1 800-255-2500
• Email: xx@xx.xx
• Phone: 1 800-255-2500
• Email: xx@xx.xx
• Phone: 1 800-255-2500
• Email: xx@xx.xx
• Phone: 1 800-255-2500
• Email: xx@xx.xx
• Phone: 1 800-255-2500
• Email: xx@xx.xx
• Phone: 1 800-255-2500
• Email: xx@xx.xx
• Phone: 1 800-255-2500
• Email: xx@xx.xx
• Phone: 1 800-255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	00863176000317 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K173550

FDA Product Code

• HTN: Washer, Bolt Nut

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2020-07-01
• Device Publish Date: 2020-03-26

On-Brand Devices [Fibulink]

• 00863176000300: FGS-1000
• 00863176000324: FGS-1300
• 00863176000317: FGS-1100