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PRAMA White Implant Systems

K180365 Class II Traditional
Decision Date
2019-07-08
Sponsor / Applicant
Sweden & Martina S.P.A.

Technical Specification

510(k) Submission ID K180365
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 2019-07-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PRAMA White Implant Systems received FDA 510(k) clearance under submission number K180365, sponsored by Sweden & Martina S.P.A.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2019-07-08.

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.