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Sentry IVC Filter

K173236 Class II Traditional
Decision Date
2018-02-22
Sponsor / Applicant
Novate Medical , Ltd.

Technical Specification

510(k) Submission ID K173236
Product Code DTK
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3375
Decision Date 2018-02-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Sentry IVC Filter received FDA 510(k) clearance under submission number K173236, sponsored by Novate Medical , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2018-02-22.

Classification & Regulation

This clearance is catalogued under FDA product code DTK and 21 CFR 870.3375, within the Cardiovascular review panel as a Class II device.