meddevicedb.com FDA Device Reference

Guided Surgery Kit Cases

K241492 Class II Traditional
Decision Date
2024-08-23
Sponsor / Applicant
JJGC Indústria e Comércio de Materiais Dentários S.A.

Technical Specification

510(k) Submission ID K241492
Product Code KCT
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6850
Decision Date 2024-08-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Guided Surgery Kit Cases received FDA 510(k) clearance under submission number K241492, sponsored by JJGC Indústria e Comércio de Materiais Dentários S.A.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2024-08-23.

Classification & Regulation

This clearance is catalogued under FDA product code KCT and 21 CFR 880.6850, within the General Hospital review panel as a Class II device.