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FDA 510(k)

NAVIPRO

K-Number: K020764 · 2002-06-03

ApplicantKinamed, Inc.
Decision Date2002-06-03
Product CodeHAW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NAVIPRO is the device name listed in this FDA 510(k) record. The listed applicant is Kinamed, Inc.. It received FDA 510(k) clearance on 2002-06-03 under 510(k) number K020764. The device is classified under product code HAW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NAVIPRO?

NAVIPRO is a medical device that received FDA 510(k) clearance on 2002-06-03. The listed applicant is Kinamed, Inc.. The 510(k) number is K020764.

When did NAVIPRO receive FDA 510(k) clearance?

NAVIPRO received FDA 510(k) clearance on 2002-06-03, under 510(k) number K020764.

Who is the listed applicant for NAVIPRO?

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

What is the FDA product code for NAVIPRO?

The FDA product code for NAVIPRO is HAW.

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Other records listing Kinamed, Inc. as applicant

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.

K122049NEUROPRO LOW PROFILE CRANIAL PLATING SYSTEMK072250SUPERCABLE GRIP AND PLATE SYSTEMK050897NAVIPRO SHOULDER SOFTWARE MODULEK033668NAVIPRO KNEE SOFTWARE MODULEK032950GEM INSET PATELLAR COMPONENTK030256ISO-ELASTIC CERCLAGE SYSTEM

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Related Devices (Code: HAW)

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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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