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KIS-II IMPLANT SYSTEM/DRILLS

K944356 Class II Traditional
Decision Date
1994-12-05
Sponsor / Applicant
Implant Center of the Palm Beaches

Technical Specification

510(k) Submission ID K944356
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 1994-12-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

KIS-II IMPLANT SYSTEM/DRILLS received FDA 510(k) clearance under submission number K944356, sponsored by Implant Center of the Palm Beaches. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1994-12-05.

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.