Codman Fiducial Marker System

FDA 510(k) K953568 · Codman & Shurtleff, Inc.

Substantially Equivalent

510(k) numberK953568

Submission

Device name
Codman Fiducial Marker System
Applicant
Codman & Shurtleff, Inc.
Raynham, MA, US
Received
July 31, 1995
Decision date
February 29, 1996
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
HAW – Neurological Stereotaxic Instrument
Device class
Class II (moderate risk)
Regulation
21 CFR 882.4560
Specialty
Neurology

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Questions and answers

When was Codman Fiducial Marker System cleared by the FDA?

Codman Fiducial Marker System (K953568) received a 510(k) decision of Substantially Equivalent on February 29, 1996, 213 days after the submission was received.

What is the product code of K953568?

The FDA product code is HAW – Neurological Stereotaxic Instrument, a Class II (moderate risk) device regulated under 21 CFR 882.4560.