Vector® Hammertoe Correction System

Screw, Fixation, Bone

Nvision Biomedical Technologies, Inc

The following data is part of a premarket notification filed by Nvision Biomedical Technologies, Inc with the FDA for Vector® Hammertoe Correction System.

Pre-market Notification Details

• Device ID: K213421
• 510k Number: K213421
• Device Name: Vector® Hammertoe Correction System
• Classification: Screw, Fixation, Bone
• Applicant: Nvision Biomedical Technologies, Inc 4590 Lockhill Selma San Antonio, TX 78249
• Contact: Diana Langham
• Correspondent: Analaura Villarreal-berain; Nvision Biomedical Technologies, Inc 4590 Lockhill Selma San Antonio, TX 78249
• Product Code: HWC
• CFR Regulation Number: 888.3040 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Special
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2021-10-20
• Decision Date: 2021-11-19