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FDA 510(k)

NIM-PRS

K-Number: K024316 · 2003-01-06

ApplicantMedtronic Xomed, Inc.
Decision Date2003-01-06
Product CodeIKN
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

NIM-PRS is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Xomed, Inc.. It received FDA 510(k) clearance on 2003-01-06 under 510(k) number K024316. The device is classified under product code IKN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NIM-PRS?

NIM-PRS is a medical device that received FDA 510(k) clearance on 2003-01-06. The listed applicant is Medtronic Xomed, Inc.. The 510(k) number is K024316.

When did NIM-PRS receive FDA 510(k) clearance?

NIM-PRS received FDA 510(k) clearance on 2003-01-06, under 510(k) number K024316.

Who is the listed applicant for NIM-PRS?

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

What is the FDA product code for NIM-PRS?

The FDA product code for NIM-PRS is IKN.

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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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