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FDA 510(k)

ANEUROPLASTIC, MODEL 43-1290

K-Number: K071776 · 2007-07-26

ApplicantCodman & Shurtleff, Inc.
Decision Date2007-07-26
Product CodeJXH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ANEUROPLASTIC, MODEL 43-1290 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 2007-07-26 under 510(k) number K071776. The device is classified under product code JXH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANEUROPLASTIC, MODEL 43-1290?

ANEUROPLASTIC, MODEL 43-1290 is a medical device that received FDA 510(k) clearance on 2007-07-26. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K071776.

When did ANEUROPLASTIC, MODEL 43-1290 receive FDA 510(k) clearance?

ANEUROPLASTIC, MODEL 43-1290 received FDA 510(k) clearance on 2007-07-26, under 510(k) number K071776.

Who is the listed applicant for ANEUROPLASTIC, MODEL 43-1290?

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 ANEUROPLASTIC, MODEL 43-1290?

The FDA product code for ANEUROPLASTIC, MODEL 43-1290 is JXH.

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Related Devices (Code: JXH)

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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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