meddevicedb.com FDA Device Reference

PYROLITE CARBON ALVEOLAR MAINTEN IMPLANT

K791416 Class II Traditional
Decision Date
1979-10-09
Sponsor / Applicant
Carbomedics, Inc.

Technical Specification

510(k) Submission ID K791416
Product Code LYC
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3930
Decision Date 1979-10-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PYROLITE CARBON ALVEOLAR MAINTEN IMPLANT received FDA 510(k) clearance under submission number K791416, sponsored by Carbomedics, 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 1979-10-09.

Classification & Regulation

This clearance is catalogued under FDA product code LYC and 21 CFR 872.3930, within the Dental review panel as a Class II device.