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FDA 510(k)

CODMAN HAKIM SHUNT SYSTEMS

K-Number: K020667 · 2002-03-28

ApplicantCodman & Shurtleff, Inc.
Decision Date2002-03-28
Product CodeJXG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CODMAN HAKIM SHUNT SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is Codman & Shurtleff, Inc.. It received FDA 510(k) clearance on 2002-03-28 under 510(k) number K020667. The device is classified under product code JXG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CODMAN HAKIM SHUNT SYSTEMS?

CODMAN HAKIM SHUNT SYSTEMS is a medical device that received FDA 510(k) clearance on 2002-03-28. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K020667.

When did CODMAN HAKIM SHUNT SYSTEMS receive FDA 510(k) clearance?

CODMAN HAKIM SHUNT SYSTEMS received FDA 510(k) clearance on 2002-03-28, under 510(k) number K020667.

Who is the listed applicant for CODMAN HAKIM SHUNT SYSTEMS?

The FDA 510(k) record lists Codman & Shurtleff, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CODMAN HAKIM SHUNT SYSTEMS?

The FDA product code for CODMAN HAKIM SHUNT SYSTEMS is JXG.

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Related Devices (Code: JXG)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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