FDA 510(k)

CODMAN VPV SYSTEM, MODEL 82-3192

K-Number: K061876 · 2006-10-16

Decision Date2006-10-16

Product CodeJXG

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

CODMAN VPV SYSTEM, MODEL 82-3192 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 2006-10-16 under 510(k) number K061876. 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 VPV SYSTEM, MODEL 82-3192?

CODMAN VPV SYSTEM, MODEL 82-3192 is a medical device that received FDA 510(k) clearance on 2006-10-16. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K061876.

When did CODMAN VPV SYSTEM, MODEL 82-3192 receive FDA 510(k) clearance?

CODMAN VPV SYSTEM, MODEL 82-3192 received FDA 510(k) clearance on 2006-10-16, under 510(k) number K061876.

Who is the listed applicant for CODMAN VPV SYSTEM, MODEL 82-3192?

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 VPV SYSTEM, MODEL 82-3192?

The FDA product code for CODMAN VPV SYSTEM, MODEL 82-3192 is JXG.

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Related Devices (Code: JXG)

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Official Source

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