meddevicedb.com FDA Device Reference

SmartShape™ Healing Abutment; Wide Custom Milled Ti-Blank Abutment

K240531 Class II Traditional
Decision Date
2024-07-30
Sponsor / Applicant
BioHorizons Implant Systems, Inc.

Technical Specification

510(k) Submission ID K240531
Product Code NHA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3630
Decision Date 2024-07-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SmartShape™ Healing Abutment; Wide Custom Milled Ti-Blank Abutment received FDA 510(k) clearance under submission number K240531, 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 2024-07-30.

Classification & Regulation

This clearance is catalogued under FDA product code NHA and 21 CFR 872.3630, within the Dental review panel as a Class II device.