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FDA 510(k)

NAVIPRO KNEE SOFTWARE MODULE

K-Number: K033668 · 2004-03-11

ApplicantKinamed, Inc.
Decision Date2004-03-11
Product CodeHAW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NAVIPRO KNEE SOFTWARE MODULE is the device name listed in this FDA 510(k) record. The listed applicant is Kinamed, Inc.. It received FDA 510(k) clearance on 2004-03-11 under 510(k) number K033668. 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 KNEE SOFTWARE MODULE?

NAVIPRO KNEE SOFTWARE MODULE is a medical device that received FDA 510(k) clearance on 2004-03-11. The listed applicant is Kinamed, Inc.. The 510(k) number is K033668.

When did NAVIPRO KNEE SOFTWARE MODULE receive FDA 510(k) clearance?

NAVIPRO KNEE SOFTWARE MODULE received FDA 510(k) clearance on 2004-03-11, under 510(k) number K033668.

Who is the listed applicant for NAVIPRO KNEE SOFTWARE MODULE?

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 KNEE SOFTWARE MODULE?

The FDA product code for NAVIPRO KNEE SOFTWARE MODULE 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.

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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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