HORIZON TITANIUM SUBTALAR 9MM

GUDID 00810012480307

BIOPRO, INC.

Subtalar implant, non-bioabsorbable, sterile

• Primary Device ID: 00810012480307
• NIH Device Record Key: 627ac776-9552-49af-a94b-47e1e9bd769c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HORIZON TITANIUM SUBTALAR 9MM
• Version Model Number: 17222
• Company DUNS: 618749857
• Company Name: BIOPRO, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810012480307 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K041936

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: 2021-06-22
• Device Publish Date: 2021-06-14

On-Brand Devices [HORIZON TITANIUM SUBTALAR 9MM]

• 00810012480307: 17222
• M209172220: 17222