meddevicedb.com FDA Device Reference

INCLUDER CLAMP

K010694 Class II Traditional
Decision Date
2002-02-11
Sponsor / Applicant
Novare Surgical Systems, Inc.

Technical Specification

510(k) Submission ID K010694
Product Code DXC
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4450
Decision Date 2002-02-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INCLUDER CLAMP received FDA 510(k) clearance under submission number K010694, sponsored by Novare Surgical Systems, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2002-02-11.

Classification & Regulation

This clearance is catalogued under FDA product code DXC and 21 CFR 870.4450, within the Cardiovascular review panel as a Class II device.