meddevicedb.com FDA Device Reference

Tapered Pro Conical Implant System

K240187 Class II Traditional
Decision Date
2024-06-05
Sponsor / Applicant
BioHorizons Implant Systems, Inc.

Technical Specification

510(k) Submission ID K240187
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 2024-06-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Tapered Pro Conical Implant System received FDA 510(k) clearance under submission number K240187, sponsored by BioHorizons Implant Systems, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2024-06-05.

Classification & Regulation

This clearance is catalogued under FDA product code DZE and 21 CFR 872.3640, within the Dental review panel as a Class II device.