meddevicedb.com FDA Device Reference

IN-OVATION C

K060837 Class II Special
Decision Date
2006-04-10
Sponsor / Applicant
Dentsply International

Technical Specification

510(k) Submission ID K060837
Product Code NJM
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.5470
Decision Date 2006-04-10
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IN-OVATION C received FDA 510(k) clearance under submission number K060837, sponsored by Dentsply International. The device was reviewed via the Special premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2006-04-10.

Classification & Regulation

This clearance is catalogued under FDA product code NJM and 21 CFR 872.5470, within the Dental review panel as a Class II device.