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FDA 510(k)

STRYKER NAVIGATION SYSTEM - HIP MODULE

K-Number: K022365 · 2003-01-22

ApplicantStryker Instruments
Decision Date2003-01-22
Product CodeHAW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

STRYKER NAVIGATION SYSTEM - HIP MODULE is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Instruments. It received FDA 510(k) clearance on 2003-01-22 under 510(k) number K022365. 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 STRYKER NAVIGATION SYSTEM - HIP MODULE?

STRYKER NAVIGATION SYSTEM - HIP MODULE is a medical device that received FDA 510(k) clearance on 2003-01-22. The listed applicant is Stryker Instruments. The 510(k) number is K022365.

When did STRYKER NAVIGATION SYSTEM - HIP MODULE receive FDA 510(k) clearance?

STRYKER NAVIGATION SYSTEM - HIP MODULE received FDA 510(k) clearance on 2003-01-22, under 510(k) number K022365.

Who is the listed applicant for STRYKER NAVIGATION SYSTEM - HIP MODULE?

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

What is the FDA product code for STRYKER NAVIGATION SYSTEM - HIP MODULE?

The FDA product code for STRYKER NAVIGATION SYSTEM - HIP MODULE 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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