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FDA 510(k)

STRYKER NAVIGATION SYSTEM-KNEE MODULE

K-Number: K010204 · 2001-08-31

ApplicantStryker Corp.
Decision Date2001-08-31
Product CodeHAW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

STRYKER NAVIGATION SYSTEM-KNEE MODULE is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corp.. It received FDA 510(k) clearance on 2001-08-31 under 510(k) number K010204. 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-KNEE MODULE?

STRYKER NAVIGATION SYSTEM-KNEE MODULE is a medical device that received FDA 510(k) clearance on 2001-08-31. The listed applicant is Stryker Corp.. The 510(k) number is K010204.

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

STRYKER NAVIGATION SYSTEM-KNEE MODULE received FDA 510(k) clearance on 2001-08-31, under 510(k) number K010204.

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

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

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

The FDA product code for STRYKER NAVIGATION SYSTEM-KNEE MODULE is HAW.

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Other records listing Stryker Corp. as applicant

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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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