meddevicedb.com FDA Device Reference

Magseed Magnetic Marker Systtem

K173587 Class II Traditional
Decision Date
2018-02-16
Sponsor / Applicant
Endomagnetics Ltd.,

Technical Specification

510(k) Submission ID K173587
Product Code NEU
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4300
Decision Date 2018-02-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Magseed Magnetic Marker Systtem received FDA 510(k) clearance under submission number K173587, sponsored by Endomagnetics Ltd.,. 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 2018-02-16.

Classification & Regulation

This clearance is catalogued under FDA product code NEU and 21 CFR 878.4300, within the General, Plastic Surgery review panel as a Class II device.