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DIGIMATCH ROBODOC SURGICAL SYSTEM

K072629 Class II Traditional
Decision Date
2008-08-06
Sponsor / Applicant
Integrated Surgical Systems, Inc.

Technical Specification

510(k) Submission ID K072629
Product Code OJP
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.4560
Decision Date 2008-08-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DIGIMATCH ROBODOC SURGICAL SYSTEM received FDA 510(k) clearance under submission number K072629, sponsored by Integrated Surgical Systems, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2008-08-06.

Classification & Regulation

This clearance is catalogued under FDA product code OJP and 21 CFR 882.4560, within the Neurology review panel as a Class II device.