meddevicedb.com FDA Device Reference

Magnetic Surgical System

K191762 Class II Traditional
Decision Date
2020-04-01
Sponsor / Applicant
Levita Magnetics International Corp

Technical Specification

510(k) Submission ID K191762
Product Code PNL
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4815
Decision Date 2020-04-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Magnetic Surgical System received FDA 510(k) clearance under submission number K191762, sponsored by Levita Magnetics International Corp. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2020-04-01.

Classification & Regulation

This clearance is catalogued under FDA product code PNL and 21 CFR 878.4815, within the General, Plastic Surgery review panel as a Class II device.