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FDA 510(k)

MEDTRONIC ORTHOPAEDIC TRAUMA APPLICATION

K-Number: K050651 · 2005-07-27

ApplicantMedtronic Navigation, Inc.
Decision Date2005-07-27
Product CodeHAW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MEDTRONIC ORTHOPAEDIC TRAUMA APPLICATION is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Navigation, Inc.. It received FDA 510(k) clearance on 2005-07-27 under 510(k) number K050651. 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 MEDTRONIC ORTHOPAEDIC TRAUMA APPLICATION?

MEDTRONIC ORTHOPAEDIC TRAUMA APPLICATION is a medical device that received FDA 510(k) clearance on 2005-07-27. The listed applicant is Medtronic Navigation, Inc.. The 510(k) number is K050651.

When did MEDTRONIC ORTHOPAEDIC TRAUMA APPLICATION receive FDA 510(k) clearance?

MEDTRONIC ORTHOPAEDIC TRAUMA APPLICATION received FDA 510(k) clearance on 2005-07-27, under 510(k) number K050651.

Who is the listed applicant for MEDTRONIC ORTHOPAEDIC TRAUMA APPLICATION?

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

What is the FDA product code for MEDTRONIC ORTHOPAEDIC TRAUMA APPLICATION?

The FDA product code for MEDTRONIC ORTHOPAEDIC TRAUMA APPLICATION is HAW.

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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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